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Detailed endometrial immune assessment of both normal and adverse reproductive outcome populations
by
Marron, Kevin
, Walsh, David
, Harrity, Conor
in
Biopsy
/ CD4 antigen
/ CD56 antigen
/ CD69 antigen
/ CD8 antigen
/ Cell activation
/ Endometrium
/ Flow cytometry
/ Implantation
/ Infertility
/ Inflammation
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Miscarriage
/ Patients
/ Pregnancy
/ Reproductive failure
/ Uterus
2019
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Detailed endometrial immune assessment of both normal and adverse reproductive outcome populations
by
Marron, Kevin
, Walsh, David
, Harrity, Conor
in
Biopsy
/ CD4 antigen
/ CD56 antigen
/ CD69 antigen
/ CD8 antigen
/ Cell activation
/ Endometrium
/ Flow cytometry
/ Implantation
/ Infertility
/ Inflammation
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Miscarriage
/ Patients
/ Pregnancy
/ Reproductive failure
/ Uterus
2019
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Detailed endometrial immune assessment of both normal and adverse reproductive outcome populations
by
Marron, Kevin
, Walsh, David
, Harrity, Conor
in
Biopsy
/ CD4 antigen
/ CD56 antigen
/ CD69 antigen
/ CD8 antigen
/ Cell activation
/ Endometrium
/ Flow cytometry
/ Implantation
/ Infertility
/ Inflammation
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Miscarriage
/ Patients
/ Pregnancy
/ Reproductive failure
/ Uterus
2019
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Detailed endometrial immune assessment of both normal and adverse reproductive outcome populations
Journal Article
Detailed endometrial immune assessment of both normal and adverse reproductive outcome populations
2019
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Overview
PurposeUsing a comprehensive flow cytometric panel, do endometrial immune profiles in adverse reproductive outcomes such as repeat implantation failure (RIF) and repeat pregnancy loss (RPL) differ from each other and male-factor controls?MethodsSix-hundred and twelve patients had an endometrial biopsy to assess the immunophenotype. History on presentation was used to subdivide the population into recurrent implantation failure (RIF) [n = 178], recurrent pregnancy loss (RPL) [n = 155], primary infertility [n = 130] and secondary infertility [n = 114]. A control group was utilised for comparative purposes [n = 35] and lymphocyte subpopulations were described.ResultsDistinct lymphocyte percentage differences were noted across the populations. Relative to controls and RPL, patients with a history of RIF had significantly raised uterine NKs (53.2 vs 45.2 & 42.9%, p < 0.0001). All sub-fertile populations had increased percentage peripheral type NKs (p = 0.001), and exhibited increased CD69+ activation (p = 0.005), higher levels of B cells (p < 0.001), elevated CD4:CD8 ratio (p < 0.0001), lower T-regs (p = 0.034) and a higher proportion of Th1+ CD4s (p = 0.001). Patient aetiology confers some distinct findings, RPL; pNK, Bcells and CD4 elevated; RIF; uNK and CD56 raised while CD-8 and NK-T lowered.ConclusionsFlow cytometric endometrial evaluation has the ability to provide a rapid and objective analysis of lymphocyte subpopulations. The findings show significant variations in cellular proportions of immune cells across the patient categories relative to control tissue. The cell types involved suggest that a potential differential pro-inflammatory bias may exist in patients with a history of adverse reproductive outcomes. Immunological assessment in appropriate populations may provide insight into the underlying aetiology of some cases of reproductive failure.
Publisher
Springer Nature B.V
Subject
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