Activated T follicular helper-like cells are released into blood after oral vaccination and correlate with vaccine specific mucosal B-cell memory

• Published in: Scientific reports Vol. 8; no. 1; pp. 2729 - 15
• Main Authors: Cárdeno, Ana, Magnusson, Maria K., Quiding-Järbrink, Marianne, Lundgren, Anna
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 09.02.2018; Nature Publishing Group
• Subjects: 13/1; 13/106; 13/21; 13/31; 631/250/2152/1566/1571; 631/250/347; 631/250/590/1883; 692/308/53/2423; antibody-responses; antigen; Antigens; Blood; CD4 antigen; CXCR5 protein; dmlt adjuvant; E coli; elispot assays; enterotoxigenic escherichia-coli; etec vaccine; Helper cells; Humanities and Social Sciences; humans; Immunization; Immunoglobulin A; Immunological memory; Interleukin 21; intestinal immune-responses; Intestine; Lymphocytes B; Lymphocytes T; Microbiology in the Medical Area; Mikrobiologi inom det medicinska området; Mucosa; multidisciplinary; Phenotypes; Science; Science & Technology - Other Topics; Science (multidisciplinary); tfh cells; Vaccination; Vaccines
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-20740-3

T follicular helper (Tfh)-like cells with potent B-cell helping ability are mobilized into human circulation after parenteral vaccination and are generally held to reflect ongoing germinal center reactions. However, whether mucosal vaccination induces systemic Tfh responses and how such responses may relate to IgA production are unknown. We investigated the frequencies, phenotype and function of circulating Tfh-like CD4 + CXCR5 + T cells (cTfh) in adults receiving an oral inactivated enterotoxigenic Escherichia coli vaccine. Subjects were classified as vaccine responders or weak/non-responders based on their intestine-derived antibody-secreting cell (ASC) IgA responses to major vaccine antigens. Oral immunization induced significantly increased proportions of cTfh cells expressing the cTfh activation marker inducible costimulator (ICOS) in ASC responders, but not in weak/non-responders. Vaccination also enhanced the expression of IL-21, Th17 markers and integrin β7 by activated cTfh cells, supporting functionality and gut homing potential. cTfh cells promoted total and vaccine specific IgA production from cocultured B cells. Magnitudes of cTfh responses assessed within a week after primary vaccinations correlated with memory intestine-derived vaccine specific IgA responses 1–2 years later. We conclude that activated ICOS + Tfh-like cells are mobilized into blood after oral vaccination and may be used as biomarkers of vaccine specific mucosal memory in humans.