Skip to main content

SARS-CoV-2 infection and pulmonary tuberculosis in children and adolescents: a case-control study



The Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) pandemic has had an impact on the global tuberculosis (TB) epidemic but evidence on the possible interaction between SARS-CoV-2 and TB, especially in children and adolescents, remains limited. We aimed to evaluate the relationship between previous infection with SARS-CoV-2 and the risk of TB in children and adolescents.


An unmatched case-control study was conducted using SARS-CoV-2 unvaccinated children and adolescents recruited into two observational TB studies (Teen TB and Umoya), between November 2020 and November 2021, in Cape Town, South Africa. Sixty-four individuals with pulmonary TB (aged < 20 years) and 99 individuals without pulmonary TB (aged < 20 years) were included. Demographics and clinical data were obtained. Serum samples collected at enrolment underwent quantitative SARS-CoV-2 anti-spike immunoglobulin G (IgG) testing using the Abbott SARS-CoV-2 IgG II Quant assay. Odds ratios (ORs) for TB were estimated using unconditional logistic regression.


There was no statistically significant difference in the odds of having pulmonary TB between those who were SARS-CoV-2 IgG seropositive and those who were seronegative (adjusted OR 0.51; 95% CI: 0.23–1.11; n = 163; p = 0.09). Of those with positive SARS-CoV-2 serology indicating prior infection, baseline IgG titres were higher in individuals with TB compared to those without TB (p = 0.04) and individuals with IgG titres in the highest tertile were more likely to have pulmonary TB compared to those with IgG levels in the lowest tertile (OR: 4.00; 95%CI: 1.13– 14.21; p = 0.03).


Our study did not find convincing evidence that SARS-CoV-2 seropositivity was associated with subsequent pulmonary TB disease; however, the association between magnitude of SARS-CoV-2 IgG response and pulmonary TB warrants further investigation. Future prospective studies, evaluating the effects of sex, age and puberty on host immune responses to M. tuberculosis and SARS-CoV-2, will also provide more clarity on the interplay between these two infections.

Peer Review reports


According to the recent World Health Organization (WHO) Global TB report, over one million children younger than 15 years of age fell ill with tuberculosis (TB) in 2021 [1]. It is estimated that a quarter of these children died of TB that year. Modelling studies also suggest that 750,000 adolescents (10 to < 20 years) develop TB disease each year globally [2]. Despite these numbers, child and adolescent TB remains an area generally neglected by research and programmatic prioritisation. Moreover, the Coronavirus Disease 2019 (COVID-19) pandemic caused by Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) has had a substantial impact on the global TB epidemic. The pandemic response has led to the fragmentation of TB services (including BCG vaccination) in many countries and high COVID-19 caseloads have placed additional pressure on overburdened health services and resulted in weakened national TB programmes, resulting in a decline in people accessing TB care and treatment and a rise in estimated TB deaths globally [3].

COVID-19 and TB share similar bio-social determinants, and it is speculated that the link between these two diseases may be bi-directional [4]. Studies on Mycobacterium tuberculosis (Mtb)/SARS-CoV-2 co-infections in adults suggest that COVID-19 can occur either before, during or after TB disease diagnosis and that TB is associated with increased COVID-19 morbidity and mortality [5,6,7,8]. In children and adolescents, the association between pulmonary TB and past SARS-CoV-2 infection remains understudied. Severe COVID-19 is characterized by lymphopenia and in combination with the use of immunosuppressive medications, could potentially lead to a reduced immune response to Mtb-specific antigens. Furthermore, other viral infections such as Human Immunodeficiency Virus (HIV), influenza and measles have been described to lead to an increased risk of TB disease in children and adults by either inducing immunosuppression or by disrupting mucosal integrity and altering host immunology [9, 10]. Both SARS-CoV-2 and Mtb principally affect the respiratory system and can elicit a hyperinflammatory state in the lung. It is therefore possible that the hyperinflammatory environment, induced by SARS-CoV-2 infection, could potentially accelerate TB disease progression [11]. Indirect evidence from a recent large global cohort, which included some children and adolescents, suggests that COVID-19 may not play a major role in facilitating the progression from Mtb infection to TB disease [12]. In contrast, a recent study from South Africa showed a significantly reduced frequency of Mtb-specific CD4 T cells in the peripheral blood of individuals with COVID-19, which supports the hypothesis that COVID-19 might increase the progression to TB disease in those with latent infection [13].

Despite attempts to elucidate interactions between SARS-CoV-2 and Mtb, several uncertainties still remain. Many individuals in high TB burden settings have viable and contained Mtb infection but are asymptomatic [14]. Improved characterisation of both cell-mediated and humoral immune responses to SARS-CoV-2 infection, in those who subsequently developed TB disease, can assist in unravelling the interplay between these two diseases and may help to identify those who are at greater risk of developing TB disease. We performed a case-control study to determine whether an association exists between previous SARS-CoV-2 infection and odds of pulmonary TB disease in children and adolescents from a high TB burden setting. We also evaluated the association between the magnitude of SARS-CoV-2 Immunoglobulin G (IgG) response and odds of pulmonary TB disease.

Methods and materials

Study design and setting

An unmatched case-control study was carried out to evaluate the association between past SARS-CoV-2 infection and odds of pulmonary TB disease in children and adolescents. The study utilised baseline clinical data and serum samples collected from the participants of two prospective cohort studies in Cape Town, South Africa. Cape Town is situated in the Western Cape province of South Africa and the overall TB incidence in the province was 681/100,000 in 2015 [15].

The Teen TB study

Teen TB aimed to better understand the biology, morbidity and social contexts of adolescent TB and how these interact. The study objectives were to evaluate the relationship between baseline imaging and respiratory function in adolescents with TB, to explore the psychosocial experience of adolescents affected by drug-susceptible and multidrug-resistant TB and to explore how pubertal hormones and viral co-infections influence the immune response to Mtb. The study included adolescents (aged 10 to < 20 years) with microbiologically confirmed pulmonary TB disease and healthy individuals exposed to an infectious case of pulmonary TB in their household. Clinical data collection, chest radiography, respiratory function assessment and blood sample collection were performed at baseline. Study methods and procedures for the Teen TB study are described in detail elsewhere [16].

The Umoya child TB study

The ongoing Umoya study is a TB diagnostic study that aims to develop a comprehensive clinical, radiological and biological biorepository to evaluate future diagnostic tools and biomarkers [17]. In addition, it aims to investigate long-term lung health outcomes. The study recruits children aged < 13 years, with HIV and without HIV, that present with well-defined symptoms suggestive of pulmonary TB from Tygerberg Children’s Hospital and Karl Bremer Hospital. These hospitals are regional referral centres and serve over 30% of the City of Cape Town metropolitan population. At baseline, a standard symptomatology questionnaire is completed, and a thorough physical examination is performed. A minimum of two respiratory samples are collected for TB investigations including sputum smear microscopy, liquid culture and the molecular diagnostic test, Xpert Ultra (Cepheid, CA, U.S.A.). Chest imaging (plain film chest x-ray), tuberculin skin test (TST) and HIV antibody testing are also done at baseline. The study includes children with TB (confirmed and unconfirmed); children in which TB was ruled out after careful investigations and follow-up (symptomatic controls) and asymptomatic sibling controls. Serum samples are collected as part of the biorepository and stored for later analysis.

Study participants and sampling

The study population comprised individuals younger than 20 years of age who were recruited into the Teen TB and Umoya studies between 1 November 2020 and 1 November 2021 with available baseline demographic, clinical, laboratory and imaging data.

Individuals with TB (cases) and those without TB (controls) for the Teen TB and Umoya studies were defined as shown in Table 1. For our study, participants were classified as cases if a primary diagnosis of newly diagnosed pulmonary TB, with or without HIV co-infection, was made in a hospital or clinic and patients were within the first 14 days since diagnosis. Controls were defined as individuals younger than 20 years of age from similar epidemiological contexts as TB cases who were evaluated closely and found to not have current TB disease.

Table 1 Inclusion and exclusion criteria for Umoya and Teen TB studies

Laboratory analyses

Previous SARS-CoV-2 infection was defined as the detection of SARS-CoV-2 IgG antibodies in stored baseline serum of COVID-19 unvaccinated individuals. We also measured the magnitude of SARS-CoV-2 IgG response, using the value of the antibody titre. Baseline serum was stored as aliquots in 500 µl tubes at -80 °C until use. The specimens were tested for IgG antibodies to the SARS-CoV-2 spike protein S1 receptor-binding domain using the Abbott SARS-CoV-2 IgG II Quant chemiluminescent microparticle immunoassay (Abbott, IL, U.S.A.) on the Architect i System (Abbott). Laboratory staff from the Division of Medical Virology at Stellenbosch University (SU) performed the serological assay according to the manufacturer’s protocols, blinded to clinical characteristics. The default unit for the Abbott SARS-CoV-2 IgG II Quant assay is AU/ml; AU/ml values ≥ 50 and < 50 were defined as positive and negative, respectively, according to the manufacturer’s instructions. All tested samples were collected prior to SARS-CoV-2 vaccination roll-out for individuals aged under 18 years in South Africa.

Statistical analysis

The number of eligible child and adolescent pulmonary TB cases and controls from the Teen TB and Umoya studies, who were enrolled during the study period, determined the study population for this hypothesis generating case-control study.

Data were analysed using STATA (version 17 STATA Corp., College Station, TX, USA). Descriptive analysis was used to characterise the study population, to compare the case and control groups and to aid in identifying differences between groups with respect to potential confounders.

Univariable logistic regression was performed to calculate unadjusted odds ratios (ORs) and accompanying 95% confidence intervals (CIs) for each covariable. The Teen TB and Umoya datasets were analysed separately before analysis of the combined dataset was performed. A forwards modelling approach was utilised to determine the final multivariable model for the combined Teen TB and Umoya dataset with age and sex included in the model a priori. For SARS-CoV-2 IgG seropositive samples, boxplots were generated to present the distribution of log-transformed viral-specific IgG response values for case and control groups. A Mann-Whitney U-test was used to assess whether the distribution of SARS-CoV-2 IgG values differed between case and control groups. Associations between SARS-CoV-2 IgG levels (tertiles) and pulmonary TB disease, adjusted for age, were also investigated further using an unconditional logistic regression model. Additional analyses of the Teen TB, Umoya and combined dataset were performed using different combinations of controls (see Additional file 1).



One-hundred-and-one adolescents (10 to < 20 years of age) and 86 children (< 13 years of age) were enrolled into the Teen TB and Umoya studies between November 2020 and November 2021, respectively. Among the 86 eligible participants from the Umoya study, 24 children were excluded because insufficient volumes of stored baseline serum were available for SARS-CoV-2 IgG testing (Fig. 1).

Fig. 1
figure 1

Flow-diagram of individuals included in the case-control study

The combined dataset included 163 participants, 53% (87/163) were female and the median age was 12 years (interquartile range [IQR] 3 to 16 years). Most children and adolescents were of mixed ancestry (51%; 83/163) and 32% (52/163) lived in informal housing. 9% (14/163) were people living with HIV and 47% (76/163) were SARS-CoV-2 IgG seropositive (Table 2, Supplementary Table S2).

Table 2 Baseline socio-demographic and clinical characteristics for each study and the combined dataset by case/ control group

SARS-CoV-2 IgG serostatus and risk of pulmonary TB

There was no significant difference in the odds of pulmonary TB disease between those with positive and negative SARS-CoV-2 IgG serology in the combined dataset (unadjusted OR 0.74 95% CI: 0.40–1.40; p = 0.36) (Table 3). After adjusting for age group (four levels), sex and household size, there was no statistically significant difference in the odds of pulmonary TB disease among those who were SARS-CoV-2 IgG seropositive compared to those who were SARS-CoV-2 IgG seronegative (adjusted OR 0.51 95% CI: 0.23–1.11; n = 163, p = 0.09). There was no evidence of an interaction between SARS-CoV-2 IgG serostatus and age group (p = 0.81) or sex (p = 0.32) in the combined dataset.

Table 3 Unadjusted and adjusted estimates of the association between SARS-CoV-2 IgG serostatus and pulmonary TB disease for each study and the combined dataset

SARS-CoV-2 IgG response and risk of pulmonary TB

In the combined dataset, TB cases who were SARS-CoV-2 IgG seropositive had a median IgG value of 790 AU/ml (IQR 308 to 1605) and seropositive controls had a median IgG value of 315 AU/ml (IQR 169 to 712; p = 0.04) (Fig. 2). We did not find evidence that median IgG values differed with age group (under 10 and 10 to < 20 years) (p = 0.26) or that median values differed with sex (p = 0.09).

Fig. 2
figure 2

Log-transformed SARS-CoV-2 IgG response values for SARS-CoV-2 IgG positive cases and controls with accompanying p-value from a Mann-Whitney U-test

SARS-CoV-2 IgG values in the upper tertile of the range were associated with 4 times greater odds of having pulmonary TB disease compared with low IgG levels (95% CI: 1.13–14.21; p = 0.03; Table 4). We found evidence for the directional trend to increased risk of pulmonary TB disease with increasing SARS-CoV-2 IgG levels (p = 0.01). There was no evidence for a departure from linearity (p = 0.80).

Table 4 Odds of pulmonary TB by SARS-CoV-2 immunoglobulin G levelsa


We hypothesised that SARS-CoV-2 IgG seropositivity, as a marker of past infection, was associated with an increased odds of pulmonary TB disease in children and adolescents. After combining both Teen TB and Umoya datasets and adjusting for age group, sex and household size, we did not find convincing evidence of a relationship between previous SARS-CoV-2 infection and pulmonary TB disease. However, using IgG antibody response to the SARS-CoV-2 spike protein S1 receptor-binding domain, we showed that the magnitude of serological response to SARS-CoV-2 amongst those with serological evidence of previous infection at baseline was associated with an increased odds of pulmonary TB disease, in a dose-response manner.

To our knowledge, this is the first study to evaluate the association between past SARS-CoV-2 infection and pulmonary TB disease in children and adolescents. Our findings could, in large part, be explained by the biases associated with the types of controls selected, which likely resulted in more controls having the exposure of interest compared to cases. It is possible that hospital-based symptomatic controls from the Umoya study may have had a recent SARS-CoV-2 infection that contributed towards their need for hospital admission. Furthermore, crowded health facilities are high risk settings for acquiring respiratory infections and frequent visits to health facilities by symptomatic controls, prior to hospital admission, could have increased their risk of acquiring SARS-CoV-2. Almost half of the controls from the Teen TB study were recruited to the study later than cases; therefore, the local seroprevalence of SARS-CoV-2 at the time of control recruitment could likely have been higher compared to when cases were recruited. This assumption is supported by recent seroprevalence data from Cape Town, which showed that SARS-CoV-2 anti-nucleocapsid seropositivity increased from ~ 39% in August 2020 to almost 68% in November 2021 [19]. However, when we included recruitment period (by quarter) in the regression model there was little, if any, confounding. Additionally, a recent study from India found that adults with Mtb infection and previous SARS-CoV-2 infection exhibited increased SARS-CoV-2 IgG levels and enhanced neutralising antibody activity compared to adults without Mtb infection [20]. Given that more than 75% of adolescent Teen TB controls were Interferon Gamma Release Assay (IGRA)-positive, increased IgG concentrations could potentially have increased the chances of these adolescents having positive SARS-CoV-2 IgG serology. Despite having more IgG seropositive child and adolescent controls in this study and some adolescents being more likely to have higher IgG concentrations (Mtb infection), increasing SARS-CoV-2 IgG levels were still associated with increased odds of pulmonary TB disease after adjusting for age. However, it was not possible to adjust for sex or HIV status due to the small number of cases in the model.

While our study does not address cellular immunity, it allows for indirect inferences about the T helper (Th)-2 effector response, because a strong SARS-CoV-2 IgG response relies on adequate Th-2 effector activation [21]. A strong Th-1 response is known to protect against the development of TB disease [22, 23]. Similarly, a coordinated Th-1 immune response to SARS-CoV-2 is associated with a good prognosis and resolution of COVID-19 in adults while Th-1 hypoactivation and Th-2 overreaction, with subsequent exhaustion, has been found to be associated with a worse prognosis [24]. Younger children, which have a high risk of progressing from Mtb infection to TB disease, also have poorly functioning innate cells and a Th-2 skew [25]. Kaiko and colleagues found that when a Th effector response is polarized to Th-2, antibody production is not only stimulated but the cell-mediated immunity is also suppressed [26]. The above mechanism could explain why an increasing SARS-CoV-2 IgG response is associated with increased odds of pulmonary TB disease.

In our study, the timing of a previous SARS-CoV-2 infection and the severity of prior COVID-19 were not known for those who tested SARS-CoV-2 IgG positive. More recent infection and more severe COVID-19 have been found to trigger extensive humoral responses and can result in higher IgG titres [27, 28]. Asymptomatic SARS-CoV-2 infections likely elicit a weaker antibody response [29] and the time course and duration of humoral immune responses are potentially very different in asymptomatic SARS-CoV-2 infections [30, 31]. The absence of this information makes the interpretation of our SARS-CoV-2 IgG response findings challenging. Moreover, individuals with mild COVID-19 symptoms may have a robust mucosal immune response within the respiratory tract that controls the virus and a limited systemic immune response [32].

A strength of the study includes the use of a serology testing strategy that allows for the interpretation of an exposure-outcome temporal association. Testing serum samples from individuals with TB who were within the first 14-day since diagnosis limited the chance of detecting IgG antibodies against SARS-CoV-2 that could have been acquired after the diagnosis of pulmonary TB disease was made. However, the possibility of TB disease preceding the SARS-CoV-2 infection still exists. Another strength is the inclusion of more controls than TB cases that come from the same cohort population. Our study does also have several limitations. The study was inadequately powered to investigate the main study associations and random error cannot be excluded. The Teen TB and Umoya studies provided different control groups for our study, and it is likely that the background frequency of SARS-CoV-2 IgG seropositivity differed between control groups and the general population; therefore, the risk of selection bias was high. There is also a risk of residual confounding in this study. SARS-CoV-2 and TB share similar bio-social determinants [33] and there are likely many potential confounders that need to be considered when investigating associations between these two infections. Furthermore, potential confounders such as sex and HIV status could not be included in the model examining the association between SARS-CoV-2 IgG tertiles and TB disease due to the small number of IgG seropositive individuals with TB disease. The matching of cases and controls on key confounders such as age and sex was not possible in this study but would likely have benefitted our overall analysis and enabled adjustment for difficult to measure confounding variables (e.g., household matching). The study included children and adolescents from a high TB-burden setting in South Africa; therefore, findings can, to some extent, be generalised to other high TB-burden settings. Given that approximately one quarter of the world’s population is estimated to be infected with Mtb [14] and the ongoing nature of the SARS-CoV-2 pandemic, findings are likely generalisable to more settings. However, the grouping into SARS-CoV-2 IgG tertiles was based on IgG ranges found in our population and may not be generalisable to other populations with different SARS-CoV-2 transmission dynamics.

Improved characterisation of the shared dysregulation of immunological responses in COVID-19 and TB in blood and lung tissue will help to determine whether more severe SARS-CoV-2 infection/ COVID-19 is a risk factor for progression to TB disease or increases susceptibility to infection. For children and adolescents, large longitudinal cohorts evaluating how host immunological responses to SARS-CoV-2 and Mtb change with age, sex and puberty would also be informative.

Our study is the first study in Africa to evaluate the association between the magnitude of SARS-CoV-2-specific IgG responses and odds of pulmonary TB disease in children and adolescents and adds to the growing body of knowledge on the association between these two infections.

Data Availability

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Competing interests.

The authors declare that they have no competing interests.



Arbitrary Units


Bacillus Calmette–Guérin


Confidence Interval


Coronavirus Disease 2019


Human Immunodeficiency Virus


Immunoglobulin G


Interquartile Range


Interferon Gamma Release Assay


Likelihood Ratio Test


London School of Hygiene and Tropical Medicine


Mycobacterium Tuberculosis


National Health Laboratory Service


Odds Ratio


Severe Acute Respiratory Syndrome-Coronavirus-2


Stellenbosch University




T helper


Tuberculin Skin Test


World Health Organization


  1. World Health Organization. Global tuberculosis Report 2022. Geneva; 2022.

  2. Snow KJ, Sismanidis C, Denholm J, Sawyer SM, Graham SM. The incidence of tuberculosis among adolescents and young adults: a global estimate. Eur Respir J. 2018;51:1702352.

    Article  PubMed  Google Scholar 

  3. Migliori GB, Thong PM, Akkerman O, Alffenaar J-W, Álvarez-Navascués F, Assao-Neino MM, et al. Worldwide Effects of Coronavirus Disease Pandemic on Tuberculosis Services, January–April 2020. Emerg Infect Dis. 2020;26:2709–12.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Udwadia ZF, Vora A, Tripathi AR, Malu KN, Lange C, Sara Raju R. COVID-19 -Tuberculosis interactions: when dark forces collide. Indian J Tuberc. 2020;67:155–62.

    Article  Google Scholar 

  5. Stochino C, Villa S, Zucchi P, Parravicini P, Gori A, Raviglione MC. Clinical characteristics of COVID-19 and active tuberculosis co-infection in an italian reference hospital. Eur Respir J. 2020;56:2001708.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Tadolini M, Codecasa LR, García-García J-M, Blanc F-X, Borisov S, Alffenaar J-W, et al. Active tuberculosis, sequelae and COVID-19 co-infection: first cohort of 49 cases. Eur Respir J. 2020;56:2001398.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Tadolini M, García-García J-M, Blanc F-X, Borisov S, Goletti D, Motta I, et al. On tuberculosis and COVID-19 co-infection. Eur Respir J. 2020;56:2002328.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Boulle A, Davies M-A, Hussey H, Ismail M, Morden E, Vundle Z et al. Risk factors for Coronavirus Disease 2019 (COVID-19) death in a Population Cohort Study from the western Cape Province, South Africa. Clin Infect Dis. 2020.

  9. Durrheim DN, Crowcroft NS, Strebel PM. Measles – The epidemiology of elimination. Vaccine. 2014;32:6880–3.

    Article  PubMed  Google Scholar 

  10. Whittaker E, López-Varela E, Broderick C, Seddon JA. Examining the Complex Relationship between Tuberculosis and other Infectious Diseases in Children. Front Pediatr. 2019;7.

  11. Visca D, Ong CWM, Tiberi S, Centis R, D’Ambrosio L, Chen B, et al. Tuberculosis and COVID-19 interaction: a review of biological, clinical and public health effects. Pulmonology. 2021;27:151–65.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Tuberculosis. COVID-19 co-infection: description of the global cohort. Eur Respir J. 2022;59:2102538.

    Article  Google Scholar 

  13. Riou C, du Bruyn E, Stek C, Daroowala R, Goliath RT, Abrahams F et al. Relationship of SARS-CoV-2–specific CD4 response to COVID-19 severity and impact of HIV-1 and tuberculosis coinfection. J Clin Invest. 2021;131.

  14. Houben RMGJ, Dodd PJ. The Global Burden of Latent Tuberculosis Infection: A Re-estimation Using Mathematical Modelling. Metcalfe JZ, editor. PLOS Med. 2016;13:e1002152.

  15. Kanabus A. TB Statistics South Africa - Incidence, prevalence. 2015.

  16. Swanepoel J, Zimri K, van der Zalm MM, Hoddinott G, Palmer M, Doruyter A, et al. Understanding the biology, morbidity and social contexts of adolescent tuberculosis: a prospective observational cohort study protocol (teen TB). BMJ Open. 2022;12:e062979.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Dewandel I, van Niekerk M, Ghimenton-Walters E, Palmer M, Anthony MG, McKenzie C, et al. UMOYA: a prospective longitudinal cohort study to evaluate novel diagnostic tools and to assess long-term impact on lung health in south african children with presumptive pulmonary TB—a study protocol. BMC Pulm Med. 2023;23:97.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Graham SM, Cuevas LE, Jean-Philippe P, Browning R, Casenghi M, Detjen AK, et al. Clinical case definitions for classification of Intrathoracic Tuberculosis in Children: an update. Clin Infect Dis. 2015;61:179–87.

    Article  Google Scholar 

  19. Hussey H, Vreede H, Davies M-A, Heekes A, Kalk E, Hardie D et al. Epidemiology and outcomes of SARS-CoV-2 infection associated with anti-nucleocapsid seropositivity in Cape Town, South Africa. medRxiv [Internet]. 2022;2022.12.01.22282927. Available from:

  20. Rajamanickam A, Kumar NP, Padmapriyadarsini C, Nancy A, Selvaraj N, Karunanithi K, et al. Latent tuberculosis co-infection is associated with heightened levels of humoral, cytokine and acute phase responses in seropositive SARS-CoV-2 infection. J Infect. 2021;83:339–46.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Sekine T, Perez-Potti A, Rivera-Ballesteros O, Strålin K, Gorin J-B, Olsson A, et al. Robust T cell immunity in Convalescent individuals with asymptomatic or mild COVID-19. Cell. 2020;183:158–168e14.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Lyadova IV, Panteleev AV. Th1 and Th17 cells in tuberculosis: Protection, Pathology, and biomarkers. Mediators Inflamm. 2015;2015:1–13.

    Article  Google Scholar 

  23. Zeng G, Zhang G, Chen X. Th1 cytokines, true functional signatures for protective immunity against TB? Cell Mol Immunol. 2018;15:206–15.

    Article  CAS  PubMed  Google Scholar 

  24. Gil-Etayo FJ, Suàrez-Fernández P, Cabrera-Marante O, Arroyo D, Garcinuño S, Naranjo L et al. T-Helper cell subset response is a determining factor in COVID-19 progression. Front Cell Infect Microbiol. 2021;11.

  25. Seddon JA, Chiang SS, Esmail H, Coussens AK. The wonder years: what can Primary School Children teach us about immunity to Mycobacterium tuberculosis? Front Immunol. 2018;9.

  26. Kaiko GE, Horvat JC, Beagley KW, Hansbro PM. Immunological decision-making: how does the immune system decide to mount a helper T-cell response? Immunology. 2008;123:326–38.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Peluso MJ, Takahashi S, Hakim J, Kelly JD, Torres L, Iyer NS et al. SARS-CoV-2 antibody magnitude and detectability are driven by disease severity, timing, and assay. Sci Adv. 2021;7.

  28. Bartsch YC, Wang C, Zohar T, Fischinger S, Atyeo C, Burke JS, et al. Humoral signatures of protective and pathological SARS-CoV-2 infection in children. Nat Med. 2021;27:454–62.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Liao B, Chen Z, Zheng P, Li L, Zhuo J, Li F et al. Detection of Anti-SARS-CoV-2-S2 IgG is more sensitive than Anti-RBD IgG in identifying asymptomatic COVID-19 patients. Front Immunol. 2021;12.

  30. 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;26:1200–4.

    Article  CAS  PubMed  Google Scholar 

  31. Seow J, Graham C, Merrick B, Acors S, Pickering S, Steel KJA, et al. Longitudinal observation and decline of neutralizing antibody responses in the three months following SARS-CoV-2 infection in humans. Nat Microbiol. 2020;5:1598–607.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Butler SE, Crowley AR, Natarajan H, Xu S, Weiner JA, Bobak CA et al. Distinct features and functions of systemic and mucosal humoral immunity among SARS-CoV-2 convalescent individuals. Front Immunol. 2021;11.

  33. Pedrazzoli D, Wingfield T. Biosocial strategies to address the socioeconomic determinants and consequences of the TB and COVID-19 pandemics. Am J Trop Med Hyg. 2021;104:407–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references


We thank Shannon Wilson from the Division of Medical Virology at Stellenbosch University and National Health Laboratory Service (NHLS) at Tygerberg Hospital for preparing samples and assisting with the serological assays. The authors also thank the study participants and their families and the research staff at the Desmond Tutu TB Centre for their dedication and support.


JAS is supported by a Clinician Scientist Fellowship jointly funded by the UK Medical Research Council (MRC) and the UK Department for International Development (DFID) under the MRC/DFID Concordat agreement (MR/R007942/1). Funding for the serological assays and testing was provided by the Johnson & Johnson COVID-19 Research and Travel Fund. MMvdZ is supported by a career development grant from the EDCTP2 program supported by the European Union (TMA2019SFP-2836 TB lung-FACT2), the Fogarty International Centre of the National Institutes of Health (Award Number: K43TW011028) and South African Medical Research Council under researcher-initiated grant.

Author information

Authors and Affiliations



JAS and DAJM conceptualised the study and supervised the work. JAS and MMvdZ provided the necessary data and assisted with developing the study methodology. WP and GvZ coordinated the virological testing and provided input on appropriate assays to use. ACH and EW provided additional methodological and/or clinical advice. JS assisted with laboratory assays, analysed data and wrote the manuscript. All authors read, edited and approved the final manuscript.

Corresponding author

Correspondence to Jeremi Swanepoel.

Ethics declarations

Ethics approval and consent to participate

This research was performed in accordance with the guidelines as set out by the Declaration of Helsinki and South African Guidelines for Good Clinical Practice. Ethical approval for the project was obtained from the London School of Hygiene and Tropical Medicine (LSHTM) Research Ethics Committee (reference 26000). The SU Health Research Ethics Committee approved the protocols for the Teen TB study (N19/10/148) and Umoya study (N17/08/083). All parents/legal guardians/participants in the Teen TB and Umoya studies provided written informed consent for their data and samples to be analysed for this study.

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.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

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 The Creative Commons Public Domain Dedication waiver ( 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

Swanepoel, J., van der Zalm, M.M., Preiser, W. et al. SARS-CoV-2 infection and pulmonary tuberculosis in children and adolescents: a case-control study. BMC Infect Dis 23, 442 (2023).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: