The immune cell profile of human fallopian tubes in health and benign pathology: a systematic review

被引:9
作者
Rigby, Charlotte H. [1 ]
Aljassim, Fatima [1 ]
Powell, Simon G. [1 ]
Wyatt, James N. R. [1 ]
Hill, Christopher J. [1 ]
Hapangama, Dharani K. [1 ,2 ]
机构
[1] Univ Liverpool, Inst Life Course & Med Sci, Dept Womens & Childrens Hlth, Liverpool L8 7SS, England
[2] Liverpool Womens Hosp NHS Fdn Trust, Liverpool L8 7SS, England
关键词
Immune cells; Fallopian tube; Ectopic pregnancy; Hydrosalpinx; Systematic review; FEMALE REPRODUCTIVE-TRACT; HUMAN UTERINE TUBES; LEUKOCYTE POPULATIONS; ECTOPIC PREGNANCY; GENITAL-TRACT; GRANULATED LYMPHOCYTES; LANGERHANS CELLS; T-LYMPHOCYTES; NK CELLS; MACROPHAGES;
D O I
10.1016/j.jri.2022.103646
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The fallopian tubes (FT) play a key role in fertility by facilitating the movement of gametes to promote fertilisation and, subsequently, passage of the zygote for implantation. Histologically, the FT mucosa consists of three main cell types: secretory, ciliated and peg cells. In addition, several studies have reported the presence of immune cells. This systematic review aims to present a comprehensive analysis of the immune cell populations in the human FT, both in health and benign pathology, to promote a better understanding of tubal pathologies and their influence on infertility. A comprehensive literature search was conducted across five databases and augmented with manual citation chaining. Forty-two eligible studies were selected in accordance with PRISMA guidelines. Following screening, risk of bias assessments were conducted, data extracted and the findings presented thematically. T lymphocytes, predominantly CD8+ T cells, represent the most abundant immune cell population within the healthy FT, with B lymphocytes, macrophages, NK cells and dendritic cells also localised to the tubal mucosa. There is evidence to suggest that lymphocyte and macrophage populations are susceptible to changes in the concentration of reproductive hormones. Tubal ectopic pregnancy, salpingitis, hydrosalpinx and endometriosis are all characterised by an increased population of macrophages in comparison to healthy FT. However, given the inconsistent evidence presented between studies, and the lack of studies examining all immune cell subtypes in tubal pathologies, only limited conclusions can be formulated on pathology-specific immune cell populations, and further research is required for validation.
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页数:13
相关论文
共 65 条
[1]  
Aljassim F., 2021, IMMUNE CELL POPULATI
[2]   Characterization of the Immune Cell Repertoire in the Normal Fallopian Tube [J].
Ardighieri, Laura ;
Lonardi, Silvia ;
Moratto, Daniele ;
Facchetti, Fabio ;
Shih, Ie-Ming ;
Vermi, William ;
Kurman, Robert J. .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 2014, 33 (06) :581-591
[3]   IDENTIFICATION OF LYMPHOCYTE SUBSETS IN THE HUMAN FALLOPIAN-TUBE [J].
BOEHME, M ;
DONAT, H .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1992, 28 (02) :81-84
[4]   A 21 YEAR SURVEY OF 654 ECTOPIC PREGNANCIES [J].
BREEN, JL .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1970, 106 (07) :1004-&
[5]  
Briceag I, 2015, J Med Life, V8, P129
[6]   GRANULATED LYMPHOCYTES IN HUMAN ENDOMETRIUM - HISTOCHEMICAL AND IMMUNOHISTOCHEMICAL STUDIES [J].
BULMER, JN ;
MORRISON, L ;
LONGFELLOW, M ;
RITSON, A ;
PACE, D .
HUMAN REPRODUCTION, 1991, 6 (06) :791-798
[7]   Immune cells in the placental bed [J].
Bulmer, Judith N. ;
Williams, Paula J. ;
Lash, Gendie E. .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2010, 54 (2-3) :281-294
[8]   Human dendritic cell subsets [J].
Collin, Matthew ;
McGovern, Naomi ;
Haniffa, Muzlifah .
IMMUNOLOGY, 2013, 140 (01) :22-30
[9]   Presence of hydrosalpinx correlated to endometrial inflammatory response in vivo [J].
Copperman, Alan B. ;
Wells, Valerie ;
Luna, Martha ;
Kalir, Tamara ;
Sandler, Benjamin ;
Mukherjee, Tanmoy .
FERTILITY AND STERILITY, 2006, 86 (04) :972-976
[10]   MORPHOLOGY AND ULTRASTRUCTURE OF FALLOPIAN-TUBE EPITHELIUM AT DIFFERENT STAGES OF THE MENSTRUAL-CYCLE AND MENOPAUSE [J].
CROW, J ;
AMSO, NN ;
LEWIN, J ;
SHAW, RW .
HUMAN REPRODUCTION, 1994, 9 (12) :2224-2233