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Sero-Surveillance to Assess Immunity to Rubella and Assessment of Immunogenicity and Safety of a Single dose of Rubella Vaccine in School Girls

BACKGROUND: Rubella vaccination is not yet included in National Immunization Schedule in India. Serosurvey is frequently used to assess epidemiologic pattern of Rubella in a community. Serosurveys in different parts of India have found that 6–47% of women are susceptible for Rubella infection. The p...

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Autores principales: Sharma, Hitt, Chowdhari, Sunil, Raina, Tilak Raj, Bhardwaj, Subodh, Namjoshi, Gajanan, Parekh, Sameer
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2888342/
https://www.ncbi.nlm.nih.gov/pubmed/20606938
http://dx.doi.org/10.4103/0970-0218.62575
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author Sharma, Hitt
Chowdhari, Sunil
Raina, Tilak Raj
Bhardwaj, Subodh
Namjoshi, Gajanan
Parekh, Sameer
author_facet Sharma, Hitt
Chowdhari, Sunil
Raina, Tilak Raj
Bhardwaj, Subodh
Namjoshi, Gajanan
Parekh, Sameer
author_sort Sharma, Hitt
collection PubMed
description BACKGROUND: Rubella vaccination is not yet included in National Immunization Schedule in India. Serosurvey is frequently used to assess epidemiologic pattern of Rubella in a community. Serosurveys in different parts of India have found that 6–47% of women are susceptible for Rubella infection. The present serosurveillance was conducted in Jammu, India, in two public schools. OBJECTIVE: To determine serological status of Rubella antibodies of school girls and assessment of immunogenicity and reactogenicity of Rubella immunization in seronegative girls. MATERIALS AND METHODS: The current study was conducted to determine Rubella serostatus in peripubertal schoolgirls aged 11–18 years and also to assess immunogenicity and safety of Rubella vaccine (R-Vac) of Serum Institute of India Ltd., Pune, in seronegative girls. For screening, pre-vaccination serum Rubella IgG antibodies were determined and to assess immunogenicity of the vaccine, post-vaccination IgG antibodies were compared with pre-vaccination levels. Safety assessment was done for a period of 8 weeks, post-vaccination. RESULTS: A total of 90 (32.7%) seronegative girls were vaccinated. All girls (100%) became seropositive, post-vaccination. Clinically relevant and statistically significant increase in anti-Rubella IgG titres was observed. The adverse events were mild and self-limiting. CONCLUSIONS: R-Vac vaccine used in the study demonstrated an excellent safety and immunogenicity profile.
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spelling pubmed-28883422010-07-06 Sero-Surveillance to Assess Immunity to Rubella and Assessment of Immunogenicity and Safety of a Single dose of Rubella Vaccine in School Girls Sharma, Hitt Chowdhari, Sunil Raina, Tilak Raj Bhardwaj, Subodh Namjoshi, Gajanan Parekh, Sameer Indian J Community Med Original Article BACKGROUND: Rubella vaccination is not yet included in National Immunization Schedule in India. Serosurvey is frequently used to assess epidemiologic pattern of Rubella in a community. Serosurveys in different parts of India have found that 6–47% of women are susceptible for Rubella infection. The present serosurveillance was conducted in Jammu, India, in two public schools. OBJECTIVE: To determine serological status of Rubella antibodies of school girls and assessment of immunogenicity and reactogenicity of Rubella immunization in seronegative girls. MATERIALS AND METHODS: The current study was conducted to determine Rubella serostatus in peripubertal schoolgirls aged 11–18 years and also to assess immunogenicity and safety of Rubella vaccine (R-Vac) of Serum Institute of India Ltd., Pune, in seronegative girls. For screening, pre-vaccination serum Rubella IgG antibodies were determined and to assess immunogenicity of the vaccine, post-vaccination IgG antibodies were compared with pre-vaccination levels. Safety assessment was done for a period of 8 weeks, post-vaccination. RESULTS: A total of 90 (32.7%) seronegative girls were vaccinated. All girls (100%) became seropositive, post-vaccination. Clinically relevant and statistically significant increase in anti-Rubella IgG titres was observed. The adverse events were mild and self-limiting. CONCLUSIONS: R-Vac vaccine used in the study demonstrated an excellent safety and immunogenicity profile. Medknow Publications 2010-01 /pmc/articles/PMC2888342/ /pubmed/20606938 http://dx.doi.org/10.4103/0970-0218.62575 Text en © Indian Journal of Community Medicine http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sharma, Hitt
Chowdhari, Sunil
Raina, Tilak Raj
Bhardwaj, Subodh
Namjoshi, Gajanan
Parekh, Sameer
Sero-Surveillance to Assess Immunity to Rubella and Assessment of Immunogenicity and Safety of a Single dose of Rubella Vaccine in School Girls
title Sero-Surveillance to Assess Immunity to Rubella and Assessment of Immunogenicity and Safety of a Single dose of Rubella Vaccine in School Girls
title_full Sero-Surveillance to Assess Immunity to Rubella and Assessment of Immunogenicity and Safety of a Single dose of Rubella Vaccine in School Girls
title_fullStr Sero-Surveillance to Assess Immunity to Rubella and Assessment of Immunogenicity and Safety of a Single dose of Rubella Vaccine in School Girls
title_full_unstemmed Sero-Surveillance to Assess Immunity to Rubella and Assessment of Immunogenicity and Safety of a Single dose of Rubella Vaccine in School Girls
title_short Sero-Surveillance to Assess Immunity to Rubella and Assessment of Immunogenicity and Safety of a Single dose of Rubella Vaccine in School Girls
title_sort sero-surveillance to assess immunity to rubella and assessment of immunogenicity and safety of a single dose of rubella vaccine in school girls
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2888342/
https://www.ncbi.nlm.nih.gov/pubmed/20606938
http://dx.doi.org/10.4103/0970-0218.62575
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