2014
DOI: 10.1155/2014/579279
|View full text |Cite|
|
Sign up to set email alerts
|

Major Histocompatibility Complex I Mediates Immunological Tolerance of the Trophoblast during Pregnancy and May Mediate Rejection during Parturition

Abstract: During pregnancy in larger mammals, the maternal immune system must tolerate the fetus for months while resisting external infection. This tolerance is facilitated by immunological communication between the fetus and the mother, which is mediated by Major Histocompatibility Complex I (MHC I) proteins, by leukocytes, and by the cytokines secreted by the leukocytes. Fetal-maternal immunological communication also supports pregnancy by inducing physiological changes in the mother. If the mother “misunderstands” t… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
19
0
2

Year Published

2016
2016
2024
2024

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 24 publications
(21 citation statements)
references
References 83 publications
0
19
0
2
Order By: Relevance
“…Classical MHC are highly polymorphic, and are thus capable of presenting many different types of antigens, including paternal antigens found on invasive trophoblast cells in cattle and horses (Davies et al, 2000;Bacon et al, 2002), although trophoblast cells may also fail to express classical MHC-I molecules containing such paternal antigens. Nonclassical MHC-I proteins express a ''zero'' antigen to evade uterine natural killer cells while being recognized as self antigen by leukocytes (Rapacz-Leonard et al, 2014). MHC-I molecules are generally not expressed from cells of non-invasive regions of the human placenta or in noninvasive trophoblast cells of the placenta in ungulates (Low et al, 1990;Ramsoondar et al, 1999;Bainbridge 2000).…”
Section: Discussionmentioning
confidence: 99%
“…Classical MHC are highly polymorphic, and are thus capable of presenting many different types of antigens, including paternal antigens found on invasive trophoblast cells in cattle and horses (Davies et al, 2000;Bacon et al, 2002), although trophoblast cells may also fail to express classical MHC-I molecules containing such paternal antigens. Nonclassical MHC-I proteins express a ''zero'' antigen to evade uterine natural killer cells while being recognized as self antigen by leukocytes (Rapacz-Leonard et al, 2014). MHC-I molecules are generally not expressed from cells of non-invasive regions of the human placenta or in noninvasive trophoblast cells of the placenta in ungulates (Low et al, 1990;Ramsoondar et al, 1999;Bainbridge 2000).…”
Section: Discussionmentioning
confidence: 99%
“…Little is known about immunological activity at the feto‐maternal junction during pregnancy, but pro‐inflammatory changes have been reported when paternal antigens are expressed on inter‐placentomal areas of the fetal membranes (Joosten et al, ; Davies et al, ). This maternal‐rejection response could be modulated by the expression of MHC‐I along with paternal antigens at the time of parturition (Rapacz‐Leonard et al, ). We hypothesize that the increased estrogen‐to‐progesterone ratio facilitates this MHC‐I‐dependent inflammatory response, thus driving the process of placentome maturation.…”
Section: Separation and Expulsion Of Fetal Membranesmentioning
confidence: 99%
“…In humans, certain HLA antigens between couples in closely related populations may lead to infertility and miscarriages [29]. Many studies showed that the sharing of certain maternal-fetal or paternal HLA and BoLA antigens may influence fetal development and survival [29,30]. Similarly, in pigs, the influence of SLA-encoded genes on reproductive performances has been reported as the association between specific SLA haplotypes and genital tract development in males, ovulation rates, litter size, and piglet weight at birth and weaning [3,17,18,19,20].…”
Section: Introductionmentioning
confidence: 99%