Cognate T and B cell interaction and association of follicular helper T cells with B cell responses in Vibrio cholerae O1 infected Bangladeshi adults

Vibrio cholerae O1 can cause life threatening diarrheal disease if left untreated. T cells can play critical roles in inducing B cell mediated immunity. As the mechanism of T cell dependent B cell maturation is not well established, we hypothesized that a specific population of T (follicular helper...

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Veröffentlicht in:Microbes and infection 2019-04, Vol.21 (3-4), p.176-183
Hauptverfasser: Rashu, Rasheduzzaman, Bhuiyan, Taufiqur Rahman, Hoq, Mohammad Rubel, Hossain, Lazina, Paul, Anik, Khan, Ashraful Islam, Chowdhury, Fahima, Harris, Jason B., Ryan, Edward T., Calderwood, Stephen B., Weil, Ana A., Qadri, Firdausi
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Sprache:eng
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Zusammenfassung:Vibrio cholerae O1 can cause life threatening diarrheal disease if left untreated. T cells can play critical roles in inducing B cell mediated immunity. As the mechanism of T cell dependent B cell maturation is not well established, we hypothesized that a specific population of T (follicular helper T, Tfh) cells, are involved in B cell maturation following cholera. We found flowcytometrically that V. cholerae infection induces significant increases in circulating Tfh cells expressing B cell maturation associated protein CD40L early in disease. The increased Tfh cells expressing CD40L recognize cholera toxin most prominently, with lessened responses to V. cholerae membrane preparation (MP) and V. cholerae cytolysin (VCC). We further showed that early induction of Tfh cells and CD40L was associated with later memory B cell responses to same antigens. Lastly, we demonstrated in vitro that Tfh cells isolated after cholera can stimulate class switching of co-cultured, isolated B cells from patients with cholera, leading to production of the more durable IgG antibody isotype colorimetrically. These studies were conducted on circulating Tfh cells; future studies will be directed at examining role of Tfh cells during cholera directly in gut mucosa of biopsied samples, at the single cell level if feasible.
ISSN:1286-4579
1769-714X
1769-714X
DOI:10.1016/j.micinf.2018.12.002