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DOI 10.1111/j.1440-1746.2005.03875.x

Медицинская библиотека · Journal of gastroenterology and hepatology · 2005

Immunological alterations in pregnant women with acute hepatitis E.

Pal Rekha, Aggarwal Rakesh, Naik Subhash R, Das Vineeta, Das Siddharth, Naik Sita

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

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%.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

Для цитирования: Pal Rekha, Aggarwal Rakesh, Naik Subhash R, Das Vineeta, Das Siddharth, Naik Sita. Immunological alterations in pregnant women with acute hepatitis E.. Journal of gastroenterology and hepatology. 2005. DOI: 10.1111/j.1440-1746.2005.03875.x.

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