The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
Regulatory T-cells and immune tolerance in pregnancy: a new target for infertility treatment?
Open accessAbstract
BACKGROUND: Adaptation of the maternal immune response to accommodate the semi-allogeneic fetus is necessary for pregnancy success, and disturbances in maternal tolerance are implicated in infertility and reproductive pathologies. T regulatory (Treg) cells are a recently discovered subset of T-lymphocytes with potent suppressive activity and pivotal roles in curtailing destructive immune responses and preventing autoimmune disease. METHODS: A systematic review was undertaken of the published literature on Treg cells in the ovary, testes, uterus and gestational tissues in pregnancy, and their link with infertility, miscarriage and pathologies of pregnancy. An overview of current knowledge on the generation, activation and modes of action of Treg cells in controlling immune responses is provided, and strategies for manipulating regulatory T-cells for potential applications in reproductive medicine are discussed. RESULTS: Studies in mouse models show that Treg cells are essential for maternal tolerance of the conceptus, and that expansion of the Treg cell pool through antigen-specific and antigen non-specific pathways allows their suppressive actions to be exerted in the critical peri-implantation phase of pregnancy. In women, Treg cells accumulate in the decidua and are elevated in maternal blood from early in the first trimester. Inadequate numbers of Treg cells or their functional deficiency are linked with infertility, miscarriage and pre-eclampsia. CONCLUSIONS: The potency and wide-ranging involvement of Treg cells in immune homeostasis and disease pathology indicates the considerable potential of these cells as therapeutic agents, raising the prospect of their utility in novel treatments for reproductive pathologies.
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Cites
Foxp3 programs the development and function of CD4+CD25+ regulatory T cells
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CD127 expression inversely correlates with FoxP3 and suppressive function of human CD4+ T reg cells
Liu, W., Putnam, A. L., Xu-yu, Z., Szot, G. L., Lee, M. R., Zhu, S., Gottlieb, P. A., Kapranov, P., Gingeras, T. R., de St. Groth, B. F., et al. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20060772 · Cited by 2,606
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CD4+CD25+ Immunoregulatory T Cells
McHugh, R. S., Whitters, M. J., Piccirillo, C. A., Young, D. A., Shevach, E. M., Collins, M., & Byrne, M. C. (2002) · Immunity · doi:10.1016/s1074-7613(02)00280-7 · Cited by 1,395
Transient expression of FOXP3 in human activated nonregulatory CD4 + T cells
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“This has led to speculation that FOXP3 induction and subsequent suppression might be a default pathway in the activation of all human T-cells (Pillai and Karandikar, 2007); however, debate continues over the suppressive qualities of transiently FOXP3þ T-cells (Allan et al., 2007).”
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Cited by
The Endometrial Microbiome and Its Impact on Human Conception
Toson, B., Simon, C., & Moreno, I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23010485 · Cited by 131
Crawford, G., Ray, A., Gudi, A., Shah, A., & Homburg, R. (2015) · Human Reproduction Update · doi:10.1093/humupd/dmu052 · Cited by 124
Natural killer T cell subsets in eutopic and ectopic endometrium: a fresh look to a busy corner
Laganà, A. S., Triolo, O., Salmeri, F. M., Granese, R., Palmara, V. I., Ban Frangež, H., Vrtčnik Bokal, E., & Sofo, V. (2016) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-015-4004-7 · Cited by 67
Metadata
- Authors
- Guerin, L. R., Prins, J. R., & Robertson, S. A.
- Venue
- Human Reproduction Update
- Publisher
- Oxford University Press (OUP)
- Published
- 2009-03-11
- Volume
- 15
- Issue
- 5
- Pages
- 517-535
- ISSN
- 1355-4786 (ISSN-L)
- 1460-2369
- OpenAlex
- W2124221440
- Cited by
- 498
- References
- 16
- FWCI
- 12.22
- Type
- journal article
- Language
- en
- Open access
- hybrid
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