Author/Authors :
Tarokhian، Batoul نويسنده Acquired Immunodeficiency Research Center, Isfahan University of Medical Sciences, Isfahan, Iran , , SHERKAT، ROYA نويسنده , , NASR ESFAHANI، MOHAMMAD HOSSEIN نويسنده , , Adib، Minoo نويسنده , , Esfahani، Abbas Kiani نويسنده Department of Reproduction Biotechnology at Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran , , Ataei، Behrooz نويسنده Infectious Diseases and Tropical Medicine Research Center, Isfahan University of Medical Sciences, Isfahan ,
Abstract :
Background: Some evidence has shown a relationship between primary human cytomegalovirus
(CMV) infection and pregnancy loss. The impact of CMV infection
reactivation during pregnancy on adverse pregnancy outcomes is not completely
understood. It is proposed that altered immune response, and therefore, recurrence
or reactivation of latent CMV infection may relate to recurrent spontaneous abortion
(RSA); however, few data are available in this regard. To find out about any cell
mediated defect and reactivation of latent CMV infection in women with RPL, cellular
immunity to the virus has been evaluated by specific cytotoxic T lymphocyte
(CTL) response to CMV.
Materials and Methods: In a case control study, CTL CD107a expression and intercellular
IFN-? production in response to CMV pp65 antigen and staphylococcus
enterotoxin B (SEB) in women with RSA were assessed by flow cytometric analysis.
Forty-four cases with history of recurrent pregnancy and forty-four controls with
history of successful pregnancies were included. The FACSCaliber flow cytometer
were used for analysis.
Results: No significant difference was observed between CD107a expression and IFN-?
production in response to CMV PP65 antigen in RPL patients and control group. However,
the cytotoxic response to SEB antigen in patients with RPL was significantly lower
than control group (p=0.042).
Conclusion: The results of this study show that impaired CD107a expression and
IFN-? production as CTL response to CMV does not appear to be a major contributing
and immune incompetence factor in patients with RPL, but cytotoxic T cell
response defect to other antigens requires to be assessed further in these patients.