Abstract | PROBLEM: The immunological equilibrium at the feto-maternal interphase contributes towards late gestational diseases like growth restriction (IUGR) pre-eclampsia (PE) and hemolysis, elevated liver enzymes, low platelets ( HELLP)-syndrome. The state of activation of decidual dendritic cells (DC) has emerged as one of the central players influencing this immunological equilibrium. METHOD OF STUDY: RESULTS: We found that expression of DEC-205 and DC-SIGN was significantly upregulated in HELLP placentas, whereas expression of DC-LAMP was abrogated almost entirely. Costaining showed an interaction between DC-SIGN(+) DC and natural killer cells as well as costaining of VEGFR-1 and -2 and DC-SIGN. Pre-eclamptic and IUGR placentas showed no significant change in any of the investigated markers compared to normal controls. CONCLUSION: Our data suggest a participation of DC-mediated immunological mechanisms in HELLP syndrome.
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Authors | Christoph Scholz, Bettina Toth, Laura Santoso, Christina Kuhn, Maximilian Franz, Doris Mayr, Udo Jeschke, Klaus Friese, Barbara Schiessl |
Journal | American journal of reproductive immunology (New York, N.Y. : 1989)
(Am J Reprod Immunol)
Vol. 60
Issue 3
Pg. 238-45
(Sep 2008)
ISSN: 1046-7408 [Print] Denmark |
PMID | 18782285
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigens, CD
- Cell Adhesion Molecules
- DC-specific ICAM-3 grabbing nonintegrin
- DEC-205 receptor
- Lectins, C-Type
- Lysosome-Associated Membrane Glycoproteins
- Minor Histocompatibility Antigens
- Receptors, Cell Surface
- Receptors, Vascular Endothelial Growth Factor
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Topics |
- Antigens, CD
(metabolism)
- Cell Adhesion Molecules
(metabolism)
- Decidua
(cytology, immunology, metabolism)
- Dendritic Cells
(immunology, metabolism)
- Female
- Fetal Growth Retardation
(immunology, metabolism)
- HELLP Syndrome
(immunology, metabolism)
- Humans
- Killer Cells, Natural
(immunology)
- Lectins, C-Type
(metabolism)
- Lysosome-Associated Membrane Glycoproteins
(metabolism)
- Minor Histocompatibility Antigens
- Placentation
- Pre-Eclampsia
(immunology, metabolism)
- Pregnancy
- Receptors, Cell Surface
(metabolism)
- Receptors, Vascular Endothelial Growth Factor
(metabolism)
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