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Immunological alterations in pregnant women with acute hepatitis E.
- Source :
- Journal of Gastroenterology & Hepatology; Jul2005, Vol. 20 Issue 7, p1094-1101, 8p
- Publication Year :
- 2005
-
Abstract
- Infection with hepatitis E virus (HEV) is a major cause of acute viral hepatitis in several developing countries. Although usually self-limiting and benign, the disease is particularly severe among pregnant women, with mortality rates reaching 15–20%.Immune parameters among pregnant women with acute hepatitis E (P-HEV) were investigated and compared with those in non-pregnant patients with hepatitis E (N-HEV), and healthy pregnant (PC) and non-pregnant (NPC) women.Peripheral blood mononuclear cells (PBMC) from P-HEV patients had lower lymphocyte proliferation response to phytohemagglutinin (PHA) than those in the PC and NPC groups. A positive lymphocyte proliferation response to HEV antigen (HEVAg), a mixture of eight peptides derived from HEV proteins, was observed in 7/19 (37%) P-HEV patients, 3/9 (33%) N-HEV patients and only 2/21 (10%) PC and 2/14 (14%) NPC subjects; the stimulation indices in the P-HEV group were similar to the N-HEV group and higher than the PC group. Measurement of cytokine production by PBMC in response to PHA and HEVAg showed a reduction in production of T-helper 1 (Th1) cytokines and an increase in that of Th2 cytokines in the P-HEV group. Cytokine mRNA levels showed similar changes.These results show the existence of a Th2 bias in pregnant women with acute hepatitis E. The role of this Th2 bias in the greater severity of hepatitis E among pregnant women needs further investigation. [ABSTRACT FROM AUTHOR]
- Subjects :
- HEPATITIS E
VIRAL hepatitis
VIRUS diseases
IMMUNOLOGY
PREGNANCY
MESSENGER RNA
Subjects
Details
- Language :
- English
- ISSN :
- 08159319
- Volume :
- 20
- Issue :
- 7
- Database :
- Complementary Index
- Journal :
- Journal of Gastroenterology & Hepatology
- Publication Type :
- Academic Journal
- Accession number :
- 17198938
- Full Text :
- https://doi.org/10.1111/j.1440-1746.2005.03875.x