A Mycobacterium tuberculosis Specific IgG3 Signature of Recurrent Tuberculosis

South Africa has the highest prevalence of HIV and tuberculosis (TB) co-infection globally. Recurrent TB, caused by relapse or reinfection, makes up the majority of TB cases in South Africa, and HIV infected individuals have a greater likelihood of developing recurrent TB. Given that TB remains a le...

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Veröffentlicht in:Frontiers in immunology 2021-09, Vol.12, p.729186-729186
Hauptverfasser: Fischinger, Stephanie, Cizmeci, Deniz, Shin, Sally, Davies, Leela, Grace, Patricia S, Sivro, Aida, Yende-Zuma, Nonhlanhla, Streeck, Hendrik, Fortune, Sarah M, Lauffenburger, Douglas A, Naidoo, Kogieleum, Alter, Galit
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Sprache:eng
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Zusammenfassung:South Africa has the highest prevalence of HIV and tuberculosis (TB) co-infection globally. Recurrent TB, caused by relapse or reinfection, makes up the majority of TB cases in South Africa, and HIV infected individuals have a greater likelihood of developing recurrent TB. Given that TB remains a leading cause of death for HIV infected individuals, and correlates of TB recurrence protection/risk have yet to be defined, here we sought to understand the antibody associated mechanisms of recurrent TB by investigating the humoral response in a longitudinal cohort of HIV co-infected individuals previously treated for TB with and without recurrent disease during follow-up, in order to identify antibody correlates of protection between individuals who do not have recurrent TB and individuals who do. We used a high-throughput, "systems serology" approach to profile biophysical and functional characteristics of antibodies targeting antigens from . Differences in antibody profiles were noted between individuals with and without recurrent TB, albeit these differences were largely observed close to the time of re-diagnosis. Individuals with recurrent TB had decreased -antigen specific IgG3 titers, but not other IgG subclasses or IgA, compared to control individuals. These data point to a potential role for -specific IgG3 responses as biomarkers or direct mediators of protective immunity against recurrence.
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2021.729186