Decreased circulating T regulatory lymphocytes in obese patients undergoing bariatric surgery

PLoS One. 2018 May 14;13(5):e0197178. doi: 10.1371/journal.pone.0197178. eCollection 2018.

Abstract

Objective: It has been previously demonstrated that T lymphocytes may be involved in the development of hypertension and microvascular remodeling, and that circulating T effector lymphocytes may be increased in hypertension. In particular, Th1 and Th 17 lymphocytes may contribute to the progression of hypertension and microvascular damage while T-regulatory (Treg) lymphocytes seem to be protective in this regard. However, no data is available about patients with severe obesity, in which pronounced microvascular alterations were observed.

Design and methods: We have investigated 32 severely obese patients undergoing bariatric surgery, as well as 24 normotensive lean subjects and 12 hypertensive lean subjects undergoing an elective surgical intervention. A peripheral blood sample was obtained before surgery for assessment of CD4+ T lymphocyte subpopulations. Lymphocyte phenotype was evaluated by flow cytometry in order to assess T-effector and Treg lymphocytes.

Results: A marked reduction of several Treg subpopulations was observed in obese patients compared with controls, together with an increased in CD4+ effector memory T-effector cells.

Conclusion: In severely obese patients, Treg lymphocytes are clearly reduced and CD4+ effector memory cells are increased. It may be hypothesized that they might contribute to the development of marked microvascular alterations previously observed in these patients.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Bariatric Surgery*
  • Female
  • Humans
  • Immunologic Memory*
  • Male
  • Middle Aged
  • Obesity, Abdominal* / blood
  • Obesity, Abdominal* / immunology
  • Obesity, Abdominal* / surgery
  • Severity of Illness Index
  • T-Lymphocytes, Regulatory* / immunology
  • T-Lymphocytes, Regulatory* / metabolism
  • Th17 Cells* / immunology
  • Th17 Cells* / metabolism

Grants and funding

The authors received no specific funding for this work.