Skip to main content

Kabasura Kudineer (KSK), a poly-herbal Siddha medicine, reduced SARS-CoV-2 viral load in asymptomatic COVID-19 individuals as compared to vitamin C and zinc supplementation: findings from a prospective, exploratory, open-labeled, comparative, randomized controlled trial, Tamil Nadu, India

Abstract

Introduction

Despite several ongoing efforts in biomedicine and traditional medicine, there are no drugs or vaccines for coronavirus disease 2019 (COVID-19) as of May 2020; Kabasura Kudineer (KSK), a polyherbal formulation from India’s Siddha system of medicine, has been traditionally used for clinical presentations similar to that of COVID-19. We explored the efficacy of KSK in reducing viral load and preventing the disease progression in asymptomatic, COVID-19 cases.

Methods

A prospective, single-center, open-labeled, randomized, controlled trial was conducted in a COVID Care Centre in Chennai, India. We recruited reverse-transcription polymerase chain reaction (RT-PCR)-confirmed COVID-19 of 18 to 55 years of age, without clinical symptoms and co-morbidities. They were randomized (1:1 ratio) to KSK (60 mL twice daily for 7 days) or standard of care (7 days supplementation of vitamin C 60,000 IU morning daily and zinc 100 mg evening daily) groups. The primary outcomes were reduction in the SARS-CoV-2 load [as measured by cyclic threshold (CT) value of RT-PCR], prevention of progression of asymptomatic to symptomatic state, and changes in the immunity markers including interleukins (IL-6, IL-10, IL-2), interferon gamma (IFNγ), and tumor necrosis factor (TNF α). Siddha clinical assessment and the occurrence of adverse effects were documented as secondary outcomes. Paired t-test was used in statistical analysis.

Results

Viral load in terms of the CT value (RdRp: 95% CI = 1.89 to 5.74) declined significantly on the seventh day in the KSK group and that of the control group, more pronounced in the study group. None progressed to the symptomatic state. There was no significant difference in the biochemical parameters. We did not observe any changes in the Siddha-based clinical examination and adverse events in both groups.

Conclusion

KSK significantly reduced SARS-CoV-2 viral load among asymptomatic COVID-19 cases and did not record any adverse effect, indicating the use of KSK in the strategy against COVID-19. Larger, multi-centric trials can strengthen the current findings.

Trial registration

Clinical Trial Registry of India CTRI2020/05/025215. Registered on 16 May 2020

Peer Review reports

Background

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causing coronavirus disease 2019 (COVID-19) has affected more than 190 million people and caused 408,600 deaths globally as of 20th July 2021 [1]. Clinical symptoms of COVID-19 include mild illness (upper respiratory tract infections, fever, anorexia, malaise, muscle pain, sore throat, dyspnea, nasal congestion, headache), pneumonia, severe pneumonia, acute respiratory failure, sepsis, and septic shock [2]. Confirmatory diagnosis of COVID-19 is done through real-time reverse transcription-polymerase chain reaction assay (RT-PCR) [3]. People who are COVID-19-positive but do not exhibit any of the symptoms are termed asymptomatic [4]. These asymptomatic COVID-19 individuals could contribute to the rapid and extensive spread of SARS-CoV-2 [5]. The prevalence of asymptomatic individuals among SARS-CoV-2-infected people is about 40–45% [6].

Despite intensive ongoing efforts at drug discovery and vaccine development, there are no proven interventions, as of May 2020 [7]. Due to the novel nature of the viral infection, the trials have explored drugs/formulations from both modern and traditional medical systems [8]. In the Indian context, Ayurveda, yoga and naturopathy, Unani, Siddha, Sowa-Rigpa, and homoeopathy (collectively called as AYUSH) are traditional medical systems recognized and patronized by the government under the Indian Ministry of AYUSH. Of the AYUSH systems, Ayurveda, yoga, and Siddha systems of medicine are indigenous to India. While Ayurveda has a wider presence, the Siddha system of medicine is rooted in the southern Indian state of Tamil Nadu and is practiced in ethnic Tamil populations of the world.

The Siddha system of medicine defines Uyirthathukkal (three humors, namely Vali (Vatham), Azhal (Pitham), and Iyam (Kabam)) and Udalkattugal (Saaram, Senneer, Oon, Kozhuppu, Enbu, Moolai, Sukkilam/Suronitham) as fundamental principles of the human body and also conceptualizes unique individual body constitution of every person called as Udaliyal [9]. These traditional systems play a vital role in the management of national health care needs [10]. They advocate drugs of herbal, mineral, and animal origins for treating various diseases. Almost 360 thousand traditional formulations/practices of Ayurveda, Siddha, Unani, and Sowa-Rigpa have been transcribed into the Traditional Knowledge Digital Library in India [11]. The reported action of herbal drugs depends on the phytochemical components [12]. Non-specific targeting antiviral therapeutic methods triggered the advancement in research on plant-based antiviral agents. Herbal antiviral formulations have contributed to managing viral infections [13]. It was found after the screening of hundreds of Chinese medicinal herbs, extracts from Lycoris radiata, Artemisia annua, Pyrrosia lingua, and Lindera aggregata had anti-SARS-CoV effect [14].

In the context of COVID-19, it is important to revisit the research potential of such antiviral herbal formulations. In fact, one such Siddha classical poly-herbal formulation Nilavembu kudineer (made as a decoction) documented antiviral action against the dengue virus [15]. Herbal formulations from the Siddha system of medicine have been widely used during the times of outbreaks of dengue in Tamil Nadu, and specifically, Nilvembu kudineer is reported to have contributed to the reduction in severe outcomes due to chikungunya and dengue in Tamil Nadu during 2015 [16]. Further, many such formulations from the Siddha system of medicine have immune-stimulating and inflammation-modulating effects [17]. Hence, on the basis of such documentation in the past, an Indian advisory by the Ministry of AYUSH incorporated the role of the Siddha system of medicine for COVID-19 [18]. On the lines of the national advisory, the state of Tamil Nadu proposed the use of Siddha formulations in the management of asymptomatic and mild COVID-19 through a new scheme, called Arokkiam in which Kabasura Kudineer is one such polyherbal Siddha formulation [19].

Kabasura Kudineer (KSK) is indicated for use in Aiya suram (fever) and Aiya noigal (respiratory diseases) in the Siddha system of medicine. KSK consists of 15 herbal ingredients of which five are shown to possess antiviral activity [20]. Cucurbitacin B (− 112.09), cardiofoliolide (− 111.5), apigenin (− 98.84), and pyrethrin (− 92.98) present in the herbal decoction were found to be effective in preventing SARS-CoV-2 binding and replication [21]. Standardization of KSK has documented organoleptic characteristics, physicochemical values, thin layer chromatographic profiles, and high-performance TLC fingerprints [22]. Furthermore, toxicological studies have documented the safety of KSK [23]. KSK possesses anti-pyretic, anti-inflammatory, and anti-bacterial effects [23]. In the absence of any systematic clinical documentation of the effectiveness of KSK for COVID-19, we proposed a prospective, exploratory, randomized, controlled trial on asymptomatic COVID-19. The cycle threshold value of RT-PCR, symptoms assessment, and cytokines have been explored as outcome measures in the effectiveness studies on asymptomatic COVID-19 cases earlier [5].

In view of the above, the primary objective of the trial was to evaluate the efficacy of KSK in terms of reduction in viral load, prevention of progression of asymptomatic to symptomatic status, and any changes in the immunological markers. The secondary objectives were to assess the symptoms based on the standard Siddha Udaliyal protocol and document the adverse effects of KSK.

Methods

Study design

This was a single-center, open-labeled, randomized controlled trial in a parallel group with a 1:1 allocation ratio [24].

Cases

As per the state protocol [25], the health authorities identified high-risk individuals through contact tracing of indexed cases and screened for SARS-CoV-2 using the RT-PCR method, at the state-run COVID-19 testing centers in the capital city of Chennai, Tamil Nadu. The COVID-19-confirmed cases, without any symptoms were referred to the COVID Care Centre managed by the Government Stanley Medical College, Chennai. We recruited all asymptomatic COVID-19-positive cases aged 18 to 55 years for the trial and randomly assigned them to the control or study groups. We excluded those with diabetes, hypertension, bronchial asthma, and malignancy. Pregnant and lactating women and those participating in other COVID-19 trials were excluded.

Study setting

We did the trial at a non-hospital setting designated as COVID Care Centre and managed by the State Government Stanley Medical College, Chennai.

Interventions

Study group (KSK)

The study drug KSK is a Siddha polyherbal formulation that contains dried parts of 15 herbs in equal proportion (Table 1). The study drug was procured in the chooranam (powder) form, as a single batch for maintaining homogeneity, from the public sector company Tamil Nadu Medicinal Plants Corporation Limited (TAMPCOL). TAMPCOL is a Good Manufacturing Practices (GMP)-certified company run by the Government of Tamil Nadu, India. KSK Chooranam (powder) was manufactured as per the National Siddha Formulary of India (part I, 1st edition 1992) [26] and supplied by TAMPCOL along with a quality control certificate. A decoction was prepared by boiling 5 g of KSK Chooranam in 240 mL water and reduced to one-fourth (60 mL) and filtered through a sieve adopting the traditional method of decoction preparation. A dose of 60 mL decoction was given to the participants after food, orally in the morning and evening for 7 days.

Table 1 Composition of Kabasura Kudineer Siddha polyherbal preparation

Control group (CZ)

The patients in the control group received vitamin C (60,000 IU) and zinc tablets (100 mg) orally in the morning and evening, respectively, for 7 days.

Outcome measures

The primary outcomes were the reduction in the SARS-CoV-2 load [as measured by CT value of RT-PCR] from the baseline to seventh day of treatment, preventing the progression of asymptomatic to symptomatic state (clinical symptoms like fever, cough, and breathlessness) and changes in the immunity markers [interleukins (IL)-6, IL-10, IL-2; interferon gamma (IFNγ); and tumor necrosis factor (TNF) alpha]. COVID-19 symptoms as per standard Siddha Udaliyal assessment protocol and the occurrence of adverse effects were documented as secondary outcomes.

Clinical assessments were carried out during the entire treatment period. These included examination based on the principles of the Siddha system of medicine viz., Siddha Udaliyal (body constitution/physique) [27], Uyir thathukkal [tridosha] [Vali - (Uyirkkal (Vayu responsible for respiration), Paruvukal (Vayu responsible for circulation), Kizhnokkukkal (Vayu responsible for downward movements), Nadukkal (Vayu responsible for homeostasis), Melnokkukal (Vayu responsible for upward movements), Nagan (Vayu responsible for intellectual functions), Koorman (Vayu responsible for ophthalmic function), Kirukaran (Vayu responsible for secretory functions), Devathathan (Vayu responsible for fatigue), Thananjeyan (intracranial Vayu), Azhal (Aakkanal (Thee responsible of digestion), Vannayeri (Thee responsible of color of blood), Aattralangi (Thee responsible of cardiac functions), Olloli Thee (Thee responsible of lusture of skin), Nokkazhal (Thee responsible of vision), Iyam (Aliiyam (Iyam responsible for innate potential), Neerppiyam (Iyam responsible for digestion), Suvaikanaiyam (Iyam responsible for taste), Niraivaiyam (Iyam responsible for strengthen of sense organs), Onriyaiyam (Iyam responsible for Joint lubrication))] and Udal thathukkal (examination of Saaram (lymph), Senneer (blood), Oon (muscle), Kozhuppu (fat), Enbu (bone), Moolai (bone marrow), Sukkilam/Suronitham (sexual secretions)) [9]. Laboratory and biochemical assessments of the renal function, liver function, hemogram, inflammatory markers, electrolytes, nasopharyngeal (NP), and oropharyngeal (OP) swabs were done at baseline and on the seventh day. The NP/OP swabs were used for viral RNA detection and quantification of E-gene, RNA-dependent RNA polymerase (RdRp) {specific target for SARS-CoV-2}, and N-gene (CT value; RT PCR). Viral RNA was extracted with the Qiagen Minikit and Machine Qiacube Automated Extraction unit and Amplification, Detection, and Quantification in Rotor-Gene Q Real-Time PCR from Qiagen, Germany, using AllplexTM 2019-nCoV Assay, Seegene Inc., Seoul, Republic of Korea. Thermal cycling using six independently controlled thermal electric modules to maintain tight temperature uniformity (range 0–100 °C with an accuracy of ± 0.2 °C of the programmed target at 90 °C and a uniformity of ± 0.4 °C well to well within 10 s at arrival at 90 °C) at all points during run with efficient optimization. Adverse events were monitored daily. Clinical data was recorded on paper-based case record forms.

Sample size

We did not have prior data on the efficacy of Siddha medicine in the management of COVID-19. Hence, as an exploratory study of the efficacy of KSK on asymptomatic COVID-19 patients, we decided to recruit 30 participants in each of the two groups.

Randomization

Eligible participants were randomly assigned (1:1) to either study (KSK) or control group (CZ). The random sequence was prepared using a random number generation in a spreadsheet program by the statistician who was not directly involved in the trial. Thirty sealed opaque envelopes were prepared for each of the study and control groups. Randomization was done by selection of a sealed opaque envelope from a closed box

Statistical analysis

The primary outcome, SARS-CoV-2 viral load in terms of CT value differences, was assessed for each group. This outcome was reported as a mean difference with 95% confidence interval (CI). A comparison of the mean difference was executed using mean ± standard deviation. The secondary outcomes, safety in terms of biochemical parameters, was described using mean ± standard deviation for normally distributed values and median with its interquartile range for values which do not follow a normal distribution. We proposed descriptive statistics for reporting adverse events.

Results

As per the state guidelines, asymptomatic cases were admitted in the COVID care center (Government of Tamil Nadu). We used this setting to recruit trial participants. During the recruitment period (2–4 June 2020), a total of 87 participants were admitted in this setting. We screened the 87 and found 60 eligible and consented to participate in the trial (Fig. 1). Except for age and gender, the study and control groups were almost similar in all the baseline characteristics (Table 2). There was no significant difference in the biochemical parameters (Table 3).

Fig. 1
figure 1

Trial flowchart

Table 2 Frequency (#) of baseline characteristics of the study and control groups
Table 3 Biochemical parameters [mean (SD)] of the study group and control group before and after treatment

All the patients were asymptomatic in both groups at the baseline, and no one progressed to the symptomatic state at the end of the treatment. Viral load (as per CT value for RdRp gene) declined significantly on the seventh day in the study group as well as in the control group (Table 4). The mean difference in the CT value was more pronounced in the study group.

Table 4 Viral load (cyclic threshold value; mean) for the study group and control group before and after treatment

Of the immunological markers measured, IFNγ (range = 0–5.5 pg/mL), IL 2 (0–12 pg/mL), and TNF-alpha (0–22 pg/mL) were within normal limits in both the groups at the baseline and after 7 days. With regard to IL-6 among the study group, it was within the normal limits (0–12 pg/mL) for 20 patients while the remaining had elevated levels [mean ± SD] (107.20 ± 86.90) at baseline, and after 7 days, two participants had elevated levels [14.35 ± 2.40]. In the control group, all the patients had their IL-6 level within the normal range at the baseline and after 7 days except one (37.91 pg/mL). IL-10 levels in the study group were within the normal limits (0–5 pg/mL) in 19 patients [15.32 ± 4.39] at the baseline, whereas on the seventh day, 25 patients had an increased level [15.32 ± 4.39]. In the control group, 28 patients had an increased level of IL-10 [14.82 ± 3.18] at the baseline, and on the seventh day, 13 patients had elevated levels [13.55 ± 2.77].

In the study group, increased levels of IL-10 (n = 7) and IL-6 (n = 5) at baseline correlated with that of Vali phenotype according to the Siddha system of medicine. We did not observe any changes in the Siddha-based clinical examination parameters. There were no adverse events reported in both groups.

Discussion

We did an exploratory trial on COVID-19-confirmed asymptomatic individuals by comparing the standard of care of vitamin C/zinc supplementation with that of Kabasura kudineer, a polyherbal decoction from India’s traditional Siddha system of medicine. We found that KSK significantly reduced the viral load of SARS-CoV-2 after 7 days, when compared to the CZ group. In both groups, the asymptomatic did not progress to the symptomatic state. Additionally, there were no adverse events during the study period.

The anti-SARS-CoV-2 activity of KSK could be due to several reasons. As such, the Siddha system of medicine had been in use for infectious diseases particularly for treating ammai noi (pox viral infections) and akki noi (herpes infections) diseases for more than thousands of years [28]. The herbs as indicated in several Siddha medicine-based formulations have been documented to have multiple effects including that of antiviral activity [29]. Some of these herbal constituents work directly on the therapeutic targets, while others potentially enhance the bioavailability or counteract drug toxicity of the medicine. The constituents of KSK have been documented to have antiviral activity [15, 30,31,32]. In fact, the most recent in silico study documented the potential in the prevention and replication of SARS-CoV-2 [21]. Further, the antioxidant activity of the herbs could be another explanation for the viral reduction. Increased oxidative stress due to free radicals helps SARS-CoV-2 in replicating and producing inflammatory responses. KSK exhibited strong antioxidant activity in terms of radical scavenging potential against DPPH (IC-50, 9.29 mg/L) [33]. Vitamin C, a documented antioxidant, thus could have played the same role in the COVID-19 management [34].

In addition to antiviral activity, we documented the changes in the immunological markers. KSK might enhance the host antiviral immune responses or block the viral immune escape mechanisms, which in turn shows antiviral activity through immunoregulatory mechanisms. Phytochemicals such as flavonoids, polysaccharides, lactones, alkaloids, diterpenoids, and glycosides present in the herbs present in the KSK have been identified as immunomodulating agents [35]. Immunomodulatory actions of one such ingredient, Andrographis paniculata (Nilavembu), has in fact through in-vitro studies showed a reduction of IL-12, TNF alpha, PGE2, NO, COX-2, and iNOS in the microglia and macrophages [35]; inhibition of the production of ROS in neutrophils [36]; regulation of the production of NK cells, IFN gamma, IL-2, and TNF alpha [37]; inhibition of IL-2, IFN gamma and IL-6; reduction of IL-13, IL-4, IL-5, and Th2 cytokines in ovalbumin-induced asthma rat model [38]; and inhibition of Nf-kB binding to DNA [39]. Further, the alkaloid, andrographolide, present in Nilavembu has been documented to have diverse biological activities such as increasing cytotoxic potential of lymphocytes, decreasing the cellular and humoral adaptive immune reaction in T cells, antigen-presenting potential of dendritic cells to T cells, and pro-inflammatory proteins expression like iNOS and COX 2 [40,41,42]. Andrographolide can modulate the innate immune response and regulate the production of antibodies. Another constituent herb, Tinospora cordifolia (Seenthil), contains cordifolioside A, cordifolioside B, syringin [43], and d-glucan [44] as the main constituents, and they are having immunomodulatory activity. Evidence from in vitro study indicates that dry ginger (Zingiber officinale) has immunomodulatory effects and is an effective antimicrobial and antiviral agent [33]. Other ingredients, Adathoda vasica, Costus speciosus, Clerodendrum serratum, and Anacyclus pyrethrum, improve the humoral and cellular immunity by immunostimulatory activity [45,46,47,48], whereas Cyperus rotundus (Koraikizhangu) has been shown to modulate both cell-mediated and antibody-mediated immune responses in Wistar rats [49]. In mouse model, water extract of another herb in KSK, Syzygium aromaticum (Kirambu), inhibited macrophages to produce both IL-1beta and IL-6 [30].

The contribution of asymptomatic COVID-19 to the ongoing transmission has been documented elsewhere [6], though the magnitude is not well characterized. Contact tracing of a COVID-19-confirmed individual is a key strategy to identify asymptomatic COVID-19 individuals. Hence, as a policy, such positive individuals are advised for home quarantine. However, in a country like India, due to socio-demographic and economic reasons, the practice of strict home quarantine is difficult. Hence, in such situations with the limited evidence available from this trial, KSK, which can be prepared and consumed at the household level, seems to be a feasible option in reducing the risk of transmission for the home-quarantined COVID-19 asymptomatic individuals. However, the self-reporting of adverse events has to be insisted with high priority.

Further, clinical features and immunological assessment of asymptomatic patients have not been explored in the literature. Published studies have documented a sub-optimal immune system among asymptomatic COVID-19 individuals in terms of low levels of circulating cytokines with minimal inflammatory responses [50]. Moreover, the reported risk of death among asymptomatic patients might be due to the unidentified levels of cytokines [5]. However, such linkage needs evaluation. As such, there were no reports from India about the immunological assessment of asymptomatic patients among those admitted in COVID care centers. In the trial, we documented elevated levels of cytokines (IL-6) in the study group at baseline, and subsequent to 7 days of administration of KSK, the levels returned back to the normal limits. We could not ascertain the reasons for the different levels of cytokines in the study and control groups. Immunological findings in this study were inconclusive. This finding, nevertheless, warrants further investigation.

In the context of the Siddha system-based examination, we identified that a particular phenotype (Vali Udaliyal) individuals had elevated levels of IL-10 and IL-6 in both the study and control groups. This finding correlates well with the Siddha principle of lowered innate immunity among individuals with Vali body type [9, 51]. As all cases were asymptomatic and did not progress to the symptomatic stage, as per the Siddha fundamentals, there was no derangement of Uyrithathukkal and udal thathugal. In fact, all the Siddha parameters were within normal levels.

The reduction in viral load of SARS-CoV-2 in the KSK arm as compared to the CZ group merits discussion. RT-PCR is meant for the detection of SARS-CoV-2 viral genome in biological samples. In the public health context strategy of testing, contact tracing, and isolation, a positive RT-PCR result helps in the isolation of the COVID-19-confirmed individuals and thereby reducing chances of further transmission. CT value of RT-PCR is inversely proportional to the amount of genetic material in the biological sample. In this study, the mean CT value observed in the KSK group at the end line was 33.45 (specifically RdRp). Such a higher CT value indicates lower viral load and proportionately presumed to have reduced infectiousness. The Indian Council of Medical Research advisory stated that the CT value cutoff is 35 for RT-PCR assays on SARS-CoV-2 [52]. An increase of one unit CT value is supposed to reduce infectivity by 32% [53]. Therefore, a higher mean CT value observed at the end line in the intervention group indicates less viral load and thus indicative of lowered transmission potential.

Limitations

Our study had few limitations. As an exploratory study, findings are mostly hypothesis-generating in nature and warrant further studies. However, despite the small sample size, the comparative nature of the trial and randomization of interventions were useful in documenting the reduction in viral load over and above the decline that could be attributable to the natural decline of SARS-CoV-2 infection. Nevertheless, there were no clinical differences in both groups despite the difference documented in terms of the end line CT values. In addition, in the absence of a follow-up beyond 7 days of treatment, we do not have information on long-term direct or indirect benefits attributable to the consumption of KSK. Further studies with a larger sample size conducted in multiple centers will strengthen the findings of the current study.

Conclusion

The current exploratory study shows that KSK significantly reduces the SARS-CoV-2 viral load among confirmed asymptomatic COVID-19 cases, when compared to those who received standard of care. Further studies on KSK will explore the public health potential of Siddha medicines in this current pandemic.

Availability of data and materials

The datasets of this clinical study are available from the corresponding author on reasonable request.

References

  1. Weekly epidemiological update on COVID-19 - 20 July 2021 [Internet]. [cited 2021 Jul 22]. Available from: https://www.who.int/publications/m/item/weekly-epidemiological-update-on-covid-19%2D%2D-20-july-2021

  2. COVID19 Guidelines: National Centre for Disease Control (NCDC) [Internet]. [cited 2020 Aug 9]. Available from: https://ncdc.gov.in/index1.php?lang=1&level=1&sublinkid=703&lid=550

  3. Emery SL, Erdman DD, Bowen MD, Newton BR, Winchell JM, Meyer RF, et al. Real-time reverse transcription–polymerase chain reaction assay for SARS-associated coronavirus. Emerg Infect Dis. 2004;10(2):311–6. https://doi.org/10.3201/eid1002.030759.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Gao Z, Xu Y, Sun C, Wang X, Guo Y, Qiu S, et al. A systematic review of asymptomatic infections with COVID-19. J Microbiol Immunol Infect. 2020; 15 [cited 2020 Jul 10]; Available from: http://www.sciencedirect.com/science/article/pii/S1684118220301134.

  5. Long Q-X, Tang X-J, Shi Q-L, Li Q, Deng H-J, Yuan J, et al. Clinical and immunological assessment of asymptomatic SARS-CoV-2 infections. Nat Med. 2020;18:1–5.

    Google Scholar 

  6. Oran DP, Topol EJ. Prevalence of asymptomatic SARS-CoV-2 infection. Ann Int Med. 2020; [cited 2020 Aug 8]; Available from: https://www.acpjournals.org/doi/10.7326/M20-3012.

  7. Draft landscape of COVID-19 candidate vaccines [Internet]. [cited 2020 Aug 9]. Available from: https://www.who.int/publications/m/item/draft-landscape-of-covid-19-candidate-vaccines

  8. Zhang Q, Wang Y, Qi C, Shen L, Li J. Clinical trial analysis of 2019-nCoV therapy registered in China. J Med Virol.2020;92(6):540-545. Available from: https://doi.org/10.1002/jmv.25733,

  9. Shanmugvelu N. Noi Nadal Noi Mudal Nadal. Chennai: Department of Indian Medicine and Homoeopathy; 1967. 164 p.

    Google Scholar 

  10. Utilization of alternative systems of medicine as health care services in India: evidence on AYUSH care from NSS 2014 [Internet]. [cited 2019 Oct 22]. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417584/

  11. About TKDL [Internet]. [cited 2020 Sep 7]. Available from: http://www.tkdl.res.in/tkdl/langdefault/Common/Abouttkdl.asp?GL=Eng

  12. Parasuraman S, Thing GS, Dhanaraj SA. Polyherbal formulation: concept of Ayurveda. Pharmacogn Rev. 2014;8(16):73–80 [cited 2020 Aug 9];. Available from: http://www.phcogrev.com/article/2014/8/16/1041030973-7847134229.

    Article  Google Scholar 

  13. Natural Products in Drug Discovery and Development | Journal of Natural Products [Internet]. [cited 2020 Aug 9]. Available from: https://pubs.acs.org/doi/10.1021/np9604893

  14. Lin L-T, Hsu W-C, Lin C-C. Antiviral natural products and herbal medicines. J Tradit Complement Med. 2014;4(1):24–35. https://doi.org/10.4103/2225-4110.124335.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Jain J, Kumar A, Narayanan V, Ramaswamy RS, Sathiyarajeswaran P, Shree Devi MS, et al. Antiviral activity of ethanolic extract of Nilavembu Kudineer against dengue and chikungunya virus through in vitro evaluation. J Ayurveda Integr Med. 2019; [cited 2020 May 8]; Available from: http://www.sciencedirect.com/science/article/pii/S0975947618300731.

  16. Health & Family Welfare Department, Government of Tamil Nadu [Internet]. [cited 2020 Aug 9]. Available from: https://www.tnhealth.org/tngovin/dph/dphdbdengue.php

  17. Kumar D, Arya V, Kaur R, Bhat ZA, Gupta VK, Kumar V. A review of immunomodulators in the Indian traditional health care system. J Microbiol Immunol Infect. 2012;45(3):165–84. https://doi.org/10.1016/j.jmii.2011.09.030.

    Article  CAS  PubMed  Google Scholar 

  18. Ministry of AYUSH | [Internet]. [cited 2020 Aug 9]. Available from: https://health.ncog.gov.in/ayush-covid-dashbaord/home

  19. Government of Tamil Nadu: Government Orders | Tamil Nadu Government Portal [Internet]. [cited 2020 Sep 7]. Available from: https://www.tn.gov.in/go_view/dept/11?page=2

  20. Vanan T. A review on “Kapa Sura Kudineer” -a Siddha formulary prediction for swine flu. Int J Pharm Sci Drug Res. 2015;26:376–83.

  21. P M. Coronavirus Spike (S) Glycoprotein (2019-Ncov) Targeted Siddha medicines Kabasura Kudineer and Thonthasura Kudineer –in silico evidence for corona viral drug. Asian J Pharm Res Health Care. 2019;11(2):20-7.

  22. John A, Jayachandran R, Ethirajulu S, Sathiyarajeswaran P. Analysis of Kabasurakudineer Chooranam-a SIDDHA formula. 2015;3(9):6.

  23. Neethu D. Anti-inflammatory, antipyretic and antibacterial study of Kabasura Kudineer Choornam [Internet] [masters]. KMCH College of Pharmacy, Coimbatore; 2017 [cited 2020 Apr 26]. Available from: http://repository-tnmgrmu.ac.in/5357/

  24. Natarajan S, Anbarasi C, Sathiyarajeswaran P, Manickam P, Geetha S, Kathiravan R, et al. The efficacy of Siddha medicine, Kabasura Kudineer (KSK) compared to vitamin C & zinc (CZ) supplementation in the management of asymptomatic COVID-19 cases: a structured summary of a study protocol for a randomised controlled trial. Trials. 2020;21(1):892. https://doi.org/10.1186/s13063-020-04823-z.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Tamil Nadu Government Portal [Internet]. [cited 2020 Sep 26]. Available from: https://www.tn.gov.in/go_view/searchresult/CORONA

  26. The Siddha Formulary of India. Government of India, Ministry of Health and Family Welfare, Department of AYUSH; 1992. (1st Edition; vol. Part I).

  27. Siddha-YIABC [Internet]. [cited 2020 Sep 8]. Available from: https://www.siddhayitool.com/

  28. Traditional medicine - an overview | ScienceDirect Topics [Internet]. [cited 2020 Aug 9]. Available from: https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/traditional-medicine

  29. Rajalakshmi P, Vadivel V, Sriram S, Brindha P. Evaluation of in vitro antioxidant and anti-atherogenic properties of selected Siddha polyherbal decoctions. Int J Res Pharm Sc. 2020;11(2):1707–15. https://doi.org/10.26452/ijrps.v11i2.2072.

    Article  CAS  Google Scholar 

  30. Cortés-Rojas DF, de Souza CRF, Oliveira WP. Clove (Syzygium aromaticum): a precious spice. Asian Pacific Journal of Tropical Biomedicine. 2014;4(2):90–6. https://doi.org/10.1016/S2221-1691(14)60215-X.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Gupta PC. Biological and pharmacological properties of Terminalia chebula Retz. (Haritaki)- an overview. 4:8.

  32. Yukawa TA, Kurokawa M, Sato H, Yoshida Y, Kageyama S, Hasegawa T, et al. Prophylactic treatment of cytomegalovirus infection with traditional herbs. Antiviral Res. 1996;32(2):63–70. https://doi.org/10.1016/0166-3542(95)00978-7.

    Article  CAS  PubMed  Google Scholar 

  33. Gupta A, Chaphalkar SR. Immunopharmacological activity of Zingiber officinale on human peripheral blood mononuclear cells. Asian J. Med. Pharm. Res. 2015;5(2):13–7.

  34. Beigmohammadi MT, Bitarafan S, Hoseindokht A, Abdollahi A, Amoozadeh L, Mahmoodi Ali Abadi M, et al. Impact of vitamins A, B, C, D, and E supplementation on improvement and mortality rate in ICU patients with coronavirus-19: a structured summary of a study protocol for a randomized controlled trial. Trials. 2020;21(1):614.

    Article  CAS  Google Scholar 

  35. Jantan I, Ahmad W, SNA B. Plant-derived immunomodulators: an insight on their preclinical evaluation and clinical trials. Front Plant Sci. 2015; [cited 2020 Jul 26];6. Available from: https://www.frontiersin.org/articles/10.3389/fpls.2015.00655/full.

  36. Maiti K, Gantait A, Kakali M, Saha BP, Mukherjee PK. Therapeutic potentials of andrographolide from Andrographis paniculata: a review. Journal of Natural Remedies. 2006;6(1):1–13.

    CAS  Google Scholar 

  37. Shen Y-C, Chen C-F, Chiou W-F. Andrographolide prevents oxygen radical production by human neutrophils: possible mechanism(s) involved in its anti-inflammatory effect. Br J Pharm. 2002;135(2):399–406. https://doi.org/10.1038/sj.bjp.0704493.

    Article  CAS  Google Scholar 

  38. Rajagopal S, Kumar RA, Deevi DS, Satyanarayana C, Rajagopalan R. Andrographolide, a potential cancer therapeutic agent isolated from Andrographis paniculata. J Ex Ther Oncol. 2003;3(3):147–58. https://doi.org/10.1046/j.1359-4117.2003.01090.x.

    Article  CAS  Google Scholar 

  39. Chiou W-F, Chen C-F, Lin J-J. Mechanisms of suppression of inducible nitric oxide synthase (iNOS) expression in RAW 264.7 cells by andrographolide. Br J Pharmacol. 2000;129(8):1553–60. https://doi.org/10.1038/sj.bjp.0703191.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Wang T, Liu B, Zhang W, Wilson B, Hong J-S. Andrographolide reduces inflammation-mediated dopaminergic neurodegeneration in mesencephalic neuron-glia cultures by inhibiting microglial activation. J Pharmacol Exp Ther. 2004;308(3):975–83. https://doi.org/10.1124/jpet.103.059683.

    Article  CAS  PubMed  Google Scholar 

  41. Xia Y-F, Ye B-Q, Li Y-D, Wang J-G, He X-J, Lin X, et al. Andrographolide attenuates inflammation by inhibition of NF-κB activation through covalent modification of reduced cysteine 62 of p50. The Journal of Immunology. 2004;173(6):4207–17. https://doi.org/10.4049/jimmunol.173.6.4207.

    Article  CAS  PubMed  Google Scholar 

  42. Hidalgo MA, Romero A, Figueroa J, Cortés P, Concha II, Hancke JL, et al. Andrographolide interferes with binding of nuclear factor-κB to DNA in HL-60-derived neutrophilic cells. Br J Pharmacol. 2005;144(5):680–6. https://doi.org/10.1038/sj.bjp.0706105.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Maurya R, Wazir V, Kapil A, Kapil RS. Cordifoliosides A and B, two new phenylpropene disaccharides from Tinospora cordifolia possessing immunostimulant activity. Nat Prod Lett. 1996;8(1):7–10. https://doi.org/10.1080/10575639608043231.

    Article  CAS  Google Scholar 

  44. More P, Pai K. In vitro NADH-oxidase, NADPH-oxidase and myeloperoxidase activity of macrophages after Tinospora cordifolia (guduchi) treatment. Immunopharmacol Immunotoxicol. 2012;34(3):368–72. https://doi.org/10.3109/08923973.2011.606324.

    Article  PubMed  Google Scholar 

  45. Vinothapooshan G. Immunomodulatory activity of various extracts of Adhatoda vasica Linn. in experimental rats. Afr J Pharm Pharmacol. 2011;5(3):306–10. https://doi.org/10.5897/AJPP10.126.

    Article  Google Scholar 

  46. Immunostimulatory potential of N-butanolic fraction of hydroalcoholic extract of Costus speciosus Koen. Rhizome | International Journal of Pharmaceutical Sciences and Research [Internet]. [cited 2020 Jul 27]. Available from: https://ijpsr.com/bft-article/immunostimulatory-potential-of-n-butanolic-fraction-of-hydroalcoholic-extract-of-costus-speciosus-koen-rhizome/?view=fulltext

  47. Kumar GMS. Evaluation changes of lungs in asthmatic rats treated with aqueous and non aqueous extract of Clerodendrum serratum and theophylline. [Internet] [Master’s Thesis]. Cherraan’s College of Pharmacy, Coimbatore; 2014. Available from: http://repository-tnmgrmu.ac.in/3728/

  48. Sharma V, Thakur M, Chauhan NS, Dixit VK. Immunomodulatory activity of petroleum ether extract of Anacyclus pyrethrum. Pharm Biol. 2010;48(11):1247–54. https://doi.org/10.3109/13880201003730642.

    Article  PubMed  Google Scholar 

  49. Seo W-G, Pae H-O, Oh G-S, Chai K-Y, Kwon T-O, Yun Y-G, et al. Inhibitory effects of methanol extract of Cyperus rotundus rhizomes on nitric oxide and superoxide productions by murine macrophage cell line, RAW 264.7 cells. J Ethnopharmacol. 2001;76(1):59–64. https://doi.org/10.1016/S0378-8741(01)00221-5.

    Article  CAS  PubMed  Google Scholar 

  50. Gudbjartsson DF, Helgason A, Jonsson H, Magnusson OT, Melsted P, Norddahl GL, et al. Spread of SARS-CoV-2 in the Icelandic population. N Engl J Med. 2020 [cited 2020 Aug 9]; Available from: https://www.nejm.org/doi/10.1056/NEJMoa2006100;382(24):2302–15.

    Article  CAS  Google Scholar 

  51. Concepts of body constitution in traditional Siddha texts: a literature review | Elsevier Enhanced Reader [Internet]. [cited 2021 Jul 22]. Available from: https://reader.elsevier.com/reader/sd/pii/S0975947618310039?token=0AF15AD8249BC2628385FE4322A0E4D10FE5AE38F7EAFF4FABB12F03A0A7DC939AA7C35F5507D18B497DCE1D0966B668&originRegion=eu-west-1&originCreation=20210722171100

  52. Das P, Mondal S, Pal S, Roy S, Vidyadharan A, Dadwal R, et al. COVID diagnostics by molecular methods: a systematic review of nucleic acid based testing systems. Indian J Med Microbiol. 2021;39(3):271–8. https://doi.org/10.1016/j.ijmmb.2021.05.012.

    Article  PubMed  PubMed Central  Google Scholar 

  53. Bullard J, Dust K, Funk D, Strong JE, Alexander D, Garnett L, et al. Predicting infectious severe acute respiratory syndrome coronavirus 2 from diagnostic samples. Clin Infect Dis. 2020;71(10):2663–6. https://doi.org/10.1093/cid/ciaa638.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors acknowledge the significant support from the COVID Care Center and Government Stanley Medical College, Chennai, and Dr. Padma Venkat, Dean, School of Public Health, SRM Institute of Science and Technology, Chennai, for her mentoring in the manuscript preparation.

Other information

Ethics approval (EC/NEW/INST/2020/461/1452020) was obtained from the institutional ethics committee of the Government Stanley Medical College, Chennai.

The trial was registered in the Clinical Trial Registry of India (CTRI/2020/05/025215). Written informed consent was obtained from all eligible patients.

Funding

The research is funded by the Central Council for Research in Siddha, Ministry of AYUSH, Government of India. The funding body had no role in the design of the study; collection, analysis, and interpretation of the data; and writing of the manuscript.

Author information

Authors and Affiliations

Authors

Contributions

SN, CA, and PM initiated the study and concept development. SN, CA, PM, PS, and PB contributed to the study design. PP, MP, KK, and PB supervised the project. SN and CA obtained the necessary approvals. SN, CA, SG, RK, and PP carried out this study. SN, CA, and PM drafted the manuscript. All authors have read and approved the final manuscript.

Corresponding author

Correspondence to S. Natarajan.

Ethics declarations

Ethics approval and consent to participate

The protocol was approved by the institutional human ethics committee of the Government Stanley Medical College, Chennai, India, on May 16, 2020. All patients provided a written informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Natarajan, S., Anbarasi, C., Sathiyarajeswaran, P. et al. Kabasura Kudineer (KSK), a poly-herbal Siddha medicine, reduced SARS-CoV-2 viral load in asymptomatic COVID-19 individuals as compared to vitamin C and zinc supplementation: findings from a prospective, exploratory, open-labeled, comparative, randomized controlled trial, Tamil Nadu, India. Trials 22, 623 (2021). https://doi.org/10.1186/s13063-021-05583-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13063-021-05583-0

Keywords