Modulation of Mycobacterium tuberculosis-specific humoral immune responses is associated with Strongyloides stercoralis co-infection

PLoS Negl Trop Dis. 2017 May 1;11(5):e0005569. doi: 10.1371/journal.pntd.0005569. eCollection 2017 May.

Abstract

Background / objectives: Helminth infections are known to influence T cell responses in latent tuberculosis (LTBI). Whether helminth infections also modulate B cell responses in helminth-tuberculosis co-infection is not known.

Methods: We assessed Mycobacterium tuberculosis (Mtb)-antigen specific IgM and IgG levels, circulating levels of the B cell growth factors, BAFF and APRIL and the absolute numbers of the various B cell subsets in individuals with LTBI, LTBI with coincident Strongyloides stercoralis (Ss) infection (LTBI/Ss) and in those with Ss infection alone (Ss). We also measured the above-mentioned parameters in the LTBI-Ss group after anthelmintic therapy.

Results: Our data reveal that LTBI-Ss exhibit significantly diminished levels of Mtb-specific IgM and IgG, BAFF and APRIL levels in comparison to those with LTBI. Similarly, those with LTBI-Ss had significantly diminished numbers of all B cell subsets (naïve, immature, classical memory, activated memory, atypical memory and plasma cells) compared to those with LTBI. There was a positive correlation between Mtb-antigen specific IgM and IgG levels and BAFF and APRIL levels that were in turn related to the numbers of activated memory B cells, atypical memory B cells and plasma cells. Finally, anthelmintic treatment resulted in significantly increased levels of Mtb-antigen specific IgM and IgG levels and the numbers of each of the B cell subsets.

Conclusions: Our data, therefore, reveal that Ss infection is associated with significant modulation of Mtb-specific antibody responses, the levels of B cell growth factors and the numbers of B cells (and their component subsets).

MeSH terms

  • Adult
  • Animals
  • Antibodies, Bacterial / blood
  • B-Cell Activating Factor / blood
  • B-Lymphocyte Subsets / immunology*
  • Coinfection / immunology*
  • Cytokines / immunology
  • Female
  • Humans
  • Immunity, Humoral*
  • Immunoglobulin G / blood
  • Immunoglobulin M / blood
  • India
  • Latent Tuberculosis / immunology*
  • Male
  • Middle Aged
  • Mycobacterium tuberculosis
  • Strongyloides stercoralis
  • Strongyloidiasis / immunology*
  • Tumor Necrosis Factor Ligand Superfamily Member 13 / blood
  • Young Adult

Substances

  • Antibodies, Bacterial
  • B-Cell Activating Factor
  • Cytokines
  • Immunoglobulin G
  • Immunoglobulin M
  • TNFSF13 protein, human
  • TNFSF13B protein, human
  • Tumor Necrosis Factor Ligand Superfamily Member 13

Grants and funding

This work was funded by the Division of Intramural Research, NIAID, NIH. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.