Effect of parity on fetal and maternal microchimerism: interaction of grafts within a host?

Author:

Gammill Hilary S.12,Guthrie Katherine A.2,Aydelotte Tessa M.2,Waldorf Kristina M. Adams12,Nelson J. Lee23

Affiliation:

1. Department of Obstetrics and Gynecology, University of Washington, Seattle, WA;

2. Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA; and

3. Division of Rheumatology, University of Washington, Seattle, WA

Abstract

Abstract Small amounts of genetically foreign cells (microchimerism, Mc) traffic between a mother and fetus during pregnancy. Commonly, these grafts durably persist. For women, multiple naturally acquired Mc grafts can accrue, as they harbor Mc from their own mothers (maternal Mc, MMc) and subsequently acquire fetal Mc (FMc) through pregnancy. The nature of interactions between these naturally acquired grafts may inform, and be informed by, observations in transplantation, including the effect of noninherited maternal HLA antigens (NIMA) and double-unit cord blood transplantation (CBT). We asked whether FMc and MMc are impacted by the addition of new grafts as evaluated by increasing parity. Mc was identified by quantitative PCR for a nonshared polymorphism unique to the Mc source. Despite increasing sources of Mc, FMc did not increase with increasing parity. MMc concentration was significantly lower with increasing parity. The odds ratio for detection of MMc for 2 or more births compared with 1 birth was .11 (95% CI 0.03-0.42, P = .001). These observations suggest that interactions occur among naturally acquired grafts and are of interest in light of recent observations of graft-graft interaction resulting in predominance of 1 unit in double-unit CBT and the correlation of MMc with the NIMA effect.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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