Open AccessαEβ7, α4β7 and α4β1 integrin contributions to T cell distribution in blood, cervix and rectal tissues: Potential implications for HIV transmission
Author(s) -
Cátia T. Perciani,
Walter Jaoko,
Bashir Farah,
Mario Ostrowski,
Omu Anzala,
Kelly S. MacDonald
Publication year - 2018
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0192482
Subject(s) - integrin , cervix , rectum , immunology , cell adhesion , medicine , biology , cell , cancer research , microbiology and biotechnology , cancer , genetics
Cell surface expression of α4β7, α4β1 and αEβ7 integrins play a key role in T cell distribution. Understanding the contribution of integrins to the density and ratios of CD4 + : CD4 neg T cell at the portals of entry for HIV is of fundamental importance for the advance of more effective HIV prevention strategies. We therefore set out to characterize and compare the expression of α4β7, α4β1 and αEβ7 integrins on systemic, cervical and rectal CD4 + and CD4 neg T cells isolated from a cohort of healthy Kenyan women at low risk for sexually transmitted infections (STI) (n = 45). Here we show that blood and cervix were enriched in α4 + β1 + CD4 + T cells and α4 + β7 hi CD4 + T cells, whereas the rectum had an equal frequency of α4 + β7 hi CD4 + T cells and αE + β7 hi CD4 + T cells. Most cervical and rectal αE + β7 hi CD4 + T cells expressed CCR5 as well as CD69. Interestingly, αEβ7 was the predominant integrin expressed by CD4 neg T cells in both mucosal sites, outnumbering αE + β7 hi CD4 + T cells approximately 2-fold in the cervix and 7-fold in the rectum. The majority of αE + β7 hi CD4 neg T cells expressed CD69 at the mucosa. Taken together, our results show unique tissue-specific patterns of integrin expression. These results can help in guiding vaccine design and also the use of therapeutically targeting integrin adhesion as a means to preventing HIV.