Patterns of Expression of Vaginal T-Cell Activation Markers during Estrogen-Maintained Vaginal Candidiasis 英文参考文献.docVIP
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Patterns of Expression of Vaginal T-Cell Activation Markers during Estrogen-Maintained Vaginal Candidiasis 英文参考文献
Original article
Patterns of Expression of Vaginal T- Cell Activation Markers
during Estrogen- Maintained Vaginal Candidiasis
Ameera Al-Sadeq, MSc, Mawieh Hamad, PhD, and Khaled Abu-Elteen, PhD
the immunosuppressive activity of estrogen was furtherinvestigated by assessing the pattern of expression of cD25, cD28, cD69,
and cD152 onvaginalt cells duringestrogen-maintained vaginalcandidiasis. a precipitous and signi?cantdecrease invaginalfungal
burdentoward the end of week 3 postinfectionwas concurrentwith asigni?cantincrease invaginallymphocyte numbers. Duringthis
period, the percentage of cD3
and cD3 cells increased from 43% and 15% atday 0 to 77% and 40% atday 28 postinfection. compared with 29% cD152
vaginalt cells innaive mice, 70% of vaginalt cells were cD152 atday 28 postinfection. inconclusion, estrogen-maintained vaginal
, cD3 cD4 , cD152 , and cD28 vaginalt cells gradually and signi?cantly increased. the percentage of
+ + + + +
cD3
+
+
cD4
+
+
+
candidiasis results inpostinfectiontime-dependentchanges inthe patternof expressionof cD152, cD28, and othert-cellmarkers,
suggestingthatt cells are subjectto mixed suppressionand activationsignals.
Key words: CD28, CD152, estrogen, vaginal candidiasis, vaginal T lymphocytes
V
aginal candidiasis (VC) is now recognized as a ma-
jor health problem for women of childbearing age
immune responses converge to protect the host against fun-
gal infections (reviewed in Romani15). Intact epithelia and en-
dothelia, microbial antagonism, and antimicrobial peptides
provide the very ?rst line of defense against fungal infections.
Additionally, professional phagocytic cells (neutrophils,
monocytes, macrophages, and dendritic cells [DCs]) reduce
fungal burden by inducing oxidative and non-oxidative kill-
ing of fungi and by restricting fungal growth and infectivity.
Nonetheless, localized T cell
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