Literature DB >> 2842446

Systemic lymphoproliferative responses to rotavirus.

B M Totterdell1, J E Banatvala, I L Chrystie, G Ball, W D Cubitt.   

Abstract

In comparison with healthy adults, elderly patients and patients who had received renal transplants had significantly lower lymphoproliferative responses to rotavirus (P = 0.04, P = 0.002, respectively) and phytohaemagglutinin (P = 0.001). However, following acute rotavirus infection, elderly persons mounted good lymphoproliferative and specific antibody responses to rotavirus. No lymphoproliferative response or specific antibody to rotavirus was detected in a child with cartilage hair hypoplasia. In cord blood samples, specific antibodies were detected in the absence of a lymphoproliferative response to rotavirus. Increases in lymphoproliferative responses as well as specific antibodies were not detected in immune adult recipients of a human rotavirus vaccine (RIT 4375), but a recipient of a bovine vaccine (RIT 4237) had an increase in lymphoproliferative response to rotavirus between 13 and 28 days postvaccination. Stimulation indices for both rotavirus and phytohaemagglutinin within the vaccine groups were comparable to the healthy laboratory personnel group.

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Year:  1988        PMID: 2842446     DOI: 10.1002/jmv.1890250106

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  12 in total

1.  Rotavirus-specific T-cell responses in young prospectively followed-up children.

Authors:  M Mäkelä; J Marttila; O Simell; J Ilonen
Journal:  Clin Exp Immunol       Date:  2004-07       Impact factor: 4.330

2.  Rotavirus-specific protein synthesis is not necessary for recognition of infected cells by virus-specific cytotoxic T lymphocytes.

Authors:  P A Offit; H B Greenberg; K I Dudzik
Journal:  J Virol       Date:  1989-08       Impact factor: 5.103

Review 3.  Rotavirus gene structure and function.

Authors:  M K Estes; J Cohen
Journal:  Microbiol Rev       Date:  1989-12

4.  Identification of a T-helper cell epitope on the rotavirus VP6 protein.

Authors:  D M Baños; S Lopez; C F Arias; F R Esquivel
Journal:  J Virol       Date:  1997-01       Impact factor: 5.103

5.  Rotavirus induces proliferative response and augments non-specific cytotoxic activity of lymphocytes in humans.

Authors:  M Yasukawa; O Nakagomi; Y Kobayashi
Journal:  Clin Exp Immunol       Date:  1990-04       Impact factor: 4.330

6.  Rotavirus-specific cytotoxic T lymphocytes appear at the intestinal mucosal surface after rotavirus infection.

Authors:  P A Offit; K I Dudzik
Journal:  J Virol       Date:  1989-08       Impact factor: 5.103

7.  Memory and distribution of virus-specific cytotoxic T lymphocytes (CTLs) and CTL precursors after rotavirus infection.

Authors:  P A Offit; S L Cunningham; K I Dudzik
Journal:  J Virol       Date:  1991-03       Impact factor: 5.103

8.  In vivo role of lymphocyte subpopulations in the control of virus excretion and mucosal antibody responses of cattle infected with rotavirus.

Authors:  G Oldham; J C Bridger; C J Howard; K R Parsons
Journal:  J Virol       Date:  1993-08       Impact factor: 5.103

Review 9.  Human viral gastroenteritis.

Authors:  M L Christensen
Journal:  Clin Microbiol Rev       Date:  1989-01       Impact factor: 26.132

10.  The effect of dexamethasone-induced immunosuppression on the development of faecal antibody and recovery from and resistance to rotavirus infection.

Authors:  G Oldham; J C Bridger
Journal:  Vet Immunol Immunopathol       Date:  1992-04       Impact factor: 2.046

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