Controlled ovarian hyperstimulation in assisted reproduction: effect on the immune system
Objective: To determine how controlled ovarian hyperstimulation (COH) in assisted reproduction affects the immune system. Design: A prospective, nonrandomized, case-control study. Setting: Academic research setting. Patient(s): Women with regular menstrual cycles undergoing COH in an assisted reprod...
Saved in:
Published in | Fertility and sterility Vol. 70; no. 5; pp. 831 - 835 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.11.1998
Elsevier Science |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Objective: To determine how controlled ovarian hyperstimulation (COH) in assisted reproduction affects the immune system.
Design: A prospective, nonrandomized, case-control study.
Setting: Academic research setting.
Patient(s): Women with regular menstrual cycles undergoing COH in an assisted reproduction program.
Intervention(s): Blood samples were collected in the early and late follicular phase, at the time of ovulation, and in the luteal phase during a natural cycle, and at four times during the next cycle, which included COH and IVF.
Main Outcome Measure(s): Lymphocyte subpopulations and the differential blood count.
Result(s): In the natural cycles, a significant increase in the total numbers of lymphocytes, B cells, natural killer cells, and CD3+HLADR+ cells was observed in the late follicular phase, whereas the T helper/T suppressor cell ratio declined. In the hyperstimulated cycles, increases were seen in the total numbers of leukocytes and neutrophils on the day of hCG administration; the number of lymphocytes, monocytes, and neutrophils was increased on the day of oocyte retrieval, and the total number of leukocytes and neutrophils increased during the luteal phase.
Conclusion(s): Controlled ovarian hyperstimulation with hMG and simultaneous administration of a GnRH antagonist did not affect the immune system. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0015-0282 1556-5653 |
DOI: | 10.1016/S0015-0282(98)00282-9 |