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Immunosenescence and gender: a study in healthy Cubans

BACKGROUND: The progressive decline in the immune function during ageing is termed immunosenescence. Previous studies have reported differences between males and females in the distribution and cell responses of lymphocyte subsets. Most studies of immunosenescence have been done in populations of in...

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Autores principales: García Verdecia, Beatriz, Saavedra Hernández, Danay, Lorenzo-Luaces, Patricia, de Jesús Badía Alvarez, Teresita, Leonard Rupalé, Idrissa, Mazorra Herrera, Zaima, Crombet Ramos, Tania, Lage Dávila, Agustín
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667016/
https://www.ncbi.nlm.nih.gov/pubmed/23627933
http://dx.doi.org/10.1186/1742-4933-10-16
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author García Verdecia, Beatriz
Saavedra Hernández, Danay
Lorenzo-Luaces, Patricia
de Jesús Badía Alvarez, Teresita
Leonard Rupalé, Idrissa
Mazorra Herrera, Zaima
Crombet Ramos, Tania
Lage Dávila, Agustín
author_facet García Verdecia, Beatriz
Saavedra Hernández, Danay
Lorenzo-Luaces, Patricia
de Jesús Badía Alvarez, Teresita
Leonard Rupalé, Idrissa
Mazorra Herrera, Zaima
Crombet Ramos, Tania
Lage Dávila, Agustín
author_sort García Verdecia, Beatriz
collection PubMed
description BACKGROUND: The progressive decline in the immune function during ageing is termed immunosenescence. Previous studies have reported differences between males and females in the distribution and cell responses of lymphocyte subsets. Most studies of immunosenescence have been done in populations of industrialized countries living in a rather cold environment, and facing lower antigenic challenges such as Cytomegalovirus (CMV). The aim of this study was to determine the effect of ageing on lymphocytes in a population with a high prevalence of CMV infection in all ages, and to compare gender differences related to the immunosenescence markers. RESULTS: Different populations of peripheral blood leukocytes from healthy young and old IgG-CMV seropositive individuals were examined using flow cytometry. With age, the number and frequency of B cells and T cells significantly decreased, while highly differentiated T cells increased. Such changes were different in males and females. The age-associated decline of less differentiated lymphocyte subsets (CD19, CD4 and CD8 cells) and the increase of highly differentiated T cells were more prominent in females. In males, there were no significant changes in CD19, CD4 and CD8 subsets but there was a significant increase in the proportion of highly differentiated T cells. CONCLUSION: Shifts in lymphocyte subsets distribution were influenced by age and gender in an IgG-CMV seropositive population. These results suggest different patterns of immunosenescence in respect to gender differences. These patterns could have implications in the design of immunotherapy in the elderly.
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spelling pubmed-36670162013-05-30 Immunosenescence and gender: a study in healthy Cubans García Verdecia, Beatriz Saavedra Hernández, Danay Lorenzo-Luaces, Patricia de Jesús Badía Alvarez, Teresita Leonard Rupalé, Idrissa Mazorra Herrera, Zaima Crombet Ramos, Tania Lage Dávila, Agustín Immun Ageing Research BACKGROUND: The progressive decline in the immune function during ageing is termed immunosenescence. Previous studies have reported differences between males and females in the distribution and cell responses of lymphocyte subsets. Most studies of immunosenescence have been done in populations of industrialized countries living in a rather cold environment, and facing lower antigenic challenges such as Cytomegalovirus (CMV). The aim of this study was to determine the effect of ageing on lymphocytes in a population with a high prevalence of CMV infection in all ages, and to compare gender differences related to the immunosenescence markers. RESULTS: Different populations of peripheral blood leukocytes from healthy young and old IgG-CMV seropositive individuals were examined using flow cytometry. With age, the number and frequency of B cells and T cells significantly decreased, while highly differentiated T cells increased. Such changes were different in males and females. The age-associated decline of less differentiated lymphocyte subsets (CD19, CD4 and CD8 cells) and the increase of highly differentiated T cells were more prominent in females. In males, there were no significant changes in CD19, CD4 and CD8 subsets but there was a significant increase in the proportion of highly differentiated T cells. CONCLUSION: Shifts in lymphocyte subsets distribution were influenced by age and gender in an IgG-CMV seropositive population. These results suggest different patterns of immunosenescence in respect to gender differences. These patterns could have implications in the design of immunotherapy in the elderly. BioMed Central 2013-04-30 /pmc/articles/PMC3667016/ /pubmed/23627933 http://dx.doi.org/10.1186/1742-4933-10-16 Text en Copyright © 2013 García Verdecia et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
García Verdecia, Beatriz
Saavedra Hernández, Danay
Lorenzo-Luaces, Patricia
de Jesús Badía Alvarez, Teresita
Leonard Rupalé, Idrissa
Mazorra Herrera, Zaima
Crombet Ramos, Tania
Lage Dávila, Agustín
Immunosenescence and gender: a study in healthy Cubans
title Immunosenescence and gender: a study in healthy Cubans
title_full Immunosenescence and gender: a study in healthy Cubans
title_fullStr Immunosenescence and gender: a study in healthy Cubans
title_full_unstemmed Immunosenescence and gender: a study in healthy Cubans
title_short Immunosenescence and gender: a study in healthy Cubans
title_sort immunosenescence and gender: a study in healthy cubans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667016/
https://www.ncbi.nlm.nih.gov/pubmed/23627933
http://dx.doi.org/10.1186/1742-4933-10-16
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