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In vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and Cryptococcus neoformans
In vitro T cell function by domestic cats and cheetahs to two common pathogens, feline herpesvirus-1 (FHV-1) and Cryptococcus neoformans, was assessed. Peripheral blood mononuclear cells (PBM) were stimulated with two strains of UV-inactivated FHV-1, whole heat-killed organisms or capsular antigen o...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119742/ https://www.ncbi.nlm.nih.gov/pubmed/1317618 http://dx.doi.org/10.1016/0165-2427(92)90143-E |
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author | Miller-Edge, Michele A. Worley, Michael B. |
author_facet | Miller-Edge, Michele A. Worley, Michael B. |
author_sort | Miller-Edge, Michele A. |
collection | PubMed |
description | In vitro T cell function by domestic cats and cheetahs to two common pathogens, feline herpesvirus-1 (FHV-1) and Cryptococcus neoformans, was assessed. Peripheral blood mononuclear cells (PBM) were stimulated with two strains of UV-inactivated FHV-1, whole heat-killed organisms or capsular antigen of Cryptococcus neoformans, and proliferative responses measured. As a group, cheetah PBM responded significantly poorer than domestic cat PBM when cultured with FHV-1. However, individual cheetah responses varied widely. Supplementation of cultures with exogenous interleukin 2 (IL-2) significantly increased the level of response of individual cheetahs to both strains of FHV-1. Cheetah sera contained slightly higher neutralizing antibody titers to FHV-1 than did domestic cat sera, suggesting that B cells function adequately in cheetahs. When stimulated with Cryptococcus neoformans, both species had similar incidences of positive proliferative responses. These data demonstrate that cheetahs exhibit heterogeneous responses to specific antigens, similar to domestic cats. However, a lower group response to FHV-1 in cheetahs suggests species differences occur. In addition, level of variability in major histocompatibility complex (MHC) class I-like genes, as determined by Southern blot hybridization, does not appear to correlate with a uniform response in in vitro functional assays. Therefore, additional mechanisms influence the final outcome of the immune response. |
format | Online Article Text |
id | pubmed-7119742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71197422020-04-08 In vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and Cryptococcus neoformans Miller-Edge, Michele A. Worley, Michael B. Vet Immunol Immunopathol Article In vitro T cell function by domestic cats and cheetahs to two common pathogens, feline herpesvirus-1 (FHV-1) and Cryptococcus neoformans, was assessed. Peripheral blood mononuclear cells (PBM) were stimulated with two strains of UV-inactivated FHV-1, whole heat-killed organisms or capsular antigen of Cryptococcus neoformans, and proliferative responses measured. As a group, cheetah PBM responded significantly poorer than domestic cat PBM when cultured with FHV-1. However, individual cheetah responses varied widely. Supplementation of cultures with exogenous interleukin 2 (IL-2) significantly increased the level of response of individual cheetahs to both strains of FHV-1. Cheetah sera contained slightly higher neutralizing antibody titers to FHV-1 than did domestic cat sera, suggesting that B cells function adequately in cheetahs. When stimulated with Cryptococcus neoformans, both species had similar incidences of positive proliferative responses. These data demonstrate that cheetahs exhibit heterogeneous responses to specific antigens, similar to domestic cats. However, a lower group response to FHV-1 in cheetahs suggests species differences occur. In addition, level of variability in major histocompatibility complex (MHC) class I-like genes, as determined by Southern blot hybridization, does not appear to correlate with a uniform response in in vitro functional assays. Therefore, additional mechanisms influence the final outcome of the immune response. Published by Elsevier B.V. 1992-01-15 2002-11-13 /pmc/articles/PMC7119742/ /pubmed/1317618 http://dx.doi.org/10.1016/0165-2427(92)90143-E Text en Copyright © 1992 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Miller-Edge, Michele A. Worley, Michael B. In vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and Cryptococcus neoformans |
title | In vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and Cryptococcus neoformans |
title_full | In vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and Cryptococcus neoformans |
title_fullStr | In vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and Cryptococcus neoformans |
title_full_unstemmed | In vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and Cryptococcus neoformans |
title_short | In vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and Cryptococcus neoformans |
title_sort | in vitro responses of cheetah mononuclear cells to feline herpesvirus-1 and cryptococcus neoformans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119742/ https://www.ncbi.nlm.nih.gov/pubmed/1317618 http://dx.doi.org/10.1016/0165-2427(92)90143-E |
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