Low-dose lymphocyte immunotherapy rebalances the peripheral blood Th1/Th2/Treg paradigm in patients with unexplained recurrent miscarriage

Reprod Biol Endocrinol. 2017 Dec 16;15(1):95. doi: 10.1186/s12958-017-0315-9.

Abstract

Background: The published results regarding lymphocytes immunotherapy for unexplained recurrent miscarriage (uRM) patients are conflicting due to different screening criteria and therapeutic protocols. The objective of the present study is to evaluate the effectiveness of immunotherapy using low-dose lymphocytes in patients with uRM and Th1/Th2/Treg paradigm disorders.

Methods: Sixty-four uRM patients who received low-dose lymphocytes immunotherapy served as the immunotherapy group, while the other 35 women who did not receive the treatment served as the control group. The proportions of peripheral blood Th1 cells, Th2 cells and Treg cells; and the concentration of TGF-β1 in serum were detected by flow cytometry and enzyme-linked immunosorbent assay (ELISA), respectively, before and after the immunotherapy.

Results: The proportion of Th1 cells was significantly decreased while the proportions of Th2 cells and Treg cells were significantly increased in immunotherapy group patients after treatment. In addition, the concentration of TGF-β1 in serum was significantly higher after immunotherapy than before. Forty-three uRM patients achieved pregnancy after receiving immunotherapy and 5 patients underwent miscarriages in the immunotherapy group (11.6%, 5/43), while 8 of the 23 pregnant patients experienced a miscarriage in the control group (34.8%, 8/23; p < 0.05).

Conclusions: Low-dose lymphocyte immunotherapy is beneficial for restoring balance in the Th1/Th2/Treg paradigm and improving pregnancy outcome in uRM patients.

Trial registration: NCT03081325 . ClinicalTrials.gov . Retrospectively registered July 2015.

Keywords: Lymphocyte immunotherapy; Recurrent miscarriage; Regulatory T cells; Th1 cells; Th2 cells.

MeSH terms

  • Abortion, Habitual / blood
  • Abortion, Habitual / therapy*
  • Adult
  • Female
  • Humans
  • Immunotherapy*
  • Lymphocyte Transfusion*
  • Pregnancy
  • Pregnancy Outcome
  • T-Lymphocytes, Regulatory*
  • Th1 Cells*
  • Th2 Cells*
  • Treatment Outcome
  • Young Adult

Associated data

  • ClinicalTrials.gov/NCT03081325