Wuchereria bancrofti infection is linked to systemic activation of CD4 and CD8 T cells

PLoS Negl Trop Dis. 2019 Aug 19;13(8):e0007623. doi: 10.1371/journal.pntd.0007623. eCollection 2019 Aug.

Abstract

Background: Susceptibility to HIV has been linked to systemic CD4+ T cell activation in cohorts of seronegative individuals with high HIV-exposure risk. We recently described an increased risk of HIV transmission in individuals infected with Wuchereria bancrofti, the causative agent for lymphatic filariasis, in a prospective cohort study. However, the reason for this phenomenon needs further investigation.

Methodology/principal findings: Two-hundred and thirty-five HIV negative adults were tested using Trop Bio ELISA for detection of W. bancrofti infection and Kato Katz urine filtration and stool based RT-PCR for detection of soil transmitted helminths and schistosomiasis. FACS analysis of the fresh peripheral whole blood was used to measure T cell activation markers (HLA-DR, CD38), differentiation markers (CD45, CD27), markers for regulatory T cells (FoxP3, CD25) and the HIV entry receptor CCR5. Frequencies of activated HLA-DRpos CD4 T cells were significantly increased in subjects with W. bancrofti infection (n = 33 median: 10.71%) compared to subjects without any helminth infection (n = 42, median 6.97%, p = 0.011) or those with other helminths (Schistosoma haematobium, S. mansoni, Trichuris trichiura, Ascaris lumbricoides, hookworm) (n = 151, median 7.38%, p = 0.009). Similarly, a significant increase in HLA-DRposCD38pos CD4 T cells and effector memory cells CD4 T cells (CD45ROposCD27neg) was observed in filarial infected participants. Multivariable analyses further confirmed a link between W. bancrofti infection and systemic activation of CD4 T cells independent of age, fever, gender or other helminth infections.

Conclusions/significance: W. bancrofti infection is linked to systemic CD4 T cell activation, which may contribute to the increased susceptibility of W. bancrofti infected individuals to HIV infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Antigens, CD / analysis
  • CD4-Positive T-Lymphocytes / chemistry
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / chemistry
  • CD8-Positive T-Lymphocytes / immunology*
  • Elephantiasis, Filarial / immunology
  • Elephantiasis, Filarial / pathology*
  • Female
  • Flow Cytometry
  • HLA-DR Antigens / analysis
  • Humans
  • Lymphocyte Activation*
  • Male
  • Middle Aged
  • Prospective Studies
  • T-Lymphocyte Subsets / chemistry
  • T-Lymphocyte Subsets / immunology*
  • Wuchereria bancrofti / immunology*
  • Young Adult

Substances

  • Antigens, CD
  • HLA-DR Antigens

Grants and funding

The EMINI study was funded by the European Union (SANTE/2004/078-545 and SANTE/2006/129-931). The WHIS study received funding by the German Research Foundation (DFG grant WSA 1878/1-1) with additional support by the European Community´s Seventh Framework Programme (FP7/2007-2013 and FP7/2007-2011 und EC-GA no. 241642. The testing for W. bancrofti was supported by a grant from the German Ministry of Science (BMBF, grant number 01KA0904, Surveillance of lymphatic filariasis (SOLF)).The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.