Induction of CD8+ immune memory and enhanced inflammation in a skin inflammation model through pre‐immunization with inactivated pathogens

Abstract Laboratory mice live in specific pathogen‐free (SPF) conditions, resulting in an immature immune system comparable to that of newborns rather than adult humans or mice from pet shops. This condition may compromise their translational value. Reintroducing pathogens would lead to the uncontro...

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Main Authors: Caroline Falkenberg, Christina Bartholdy, Janne Koch, Martin Fitzner Toft, Søren Skov, Camilla Hartmann Friis Hansen, Axel Kornerup Hansen
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Clinical and Translational Science
Online Access:https://doi.org/10.1111/cts.13697
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author Caroline Falkenberg
Christina Bartholdy
Janne Koch
Martin Fitzner Toft
Søren Skov
Camilla Hartmann Friis Hansen
Axel Kornerup Hansen
author_facet Caroline Falkenberg
Christina Bartholdy
Janne Koch
Martin Fitzner Toft
Søren Skov
Camilla Hartmann Friis Hansen
Axel Kornerup Hansen
author_sort Caroline Falkenberg
collection DOAJ
description Abstract Laboratory mice live in specific pathogen‐free (SPF) conditions, resulting in an immature immune system comparable to that of newborns rather than adult humans or mice from pet shops. This condition may compromise their translational value. Reintroducing pathogens would lead to the uncontrolled spread of infections and associated diseases, so research facilities should seek safer alternatives. We immunized laboratory mice with a cocktail of pathogens, which were inactivated by ultraviolet irradiation and mixed with the adjuvant AddaVax. This immunization resulted in a higher percentage of CD8+ effector memory T cells compared to untreated mice, although the response was not as robust as in pet shop mice. In a model of skin inflammation, pre‐immunization led to an increased skin inflammatory response compared to non‐immunized mice. All immunized mice seroconverted to the pathogens in the mixture, while none of the non‐immunized mice housed together seroconverted to the pathogens applied to the pre‐immunized mice. In conclusion, pre‐immunization of mice impacts the immune system, which includes increasing the levels of CD8+ effector memory T cells.
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spelling doaj.art-17eb575ccf154419a5393edf5fb3c8b92024-01-24T18:33:50ZengWileyClinical and Translational Science1752-80541752-80622024-01-01171n/an/a10.1111/cts.13697Induction of CD8+ immune memory and enhanced inflammation in a skin inflammation model through pre‐immunization with inactivated pathogensCaroline Falkenberg0Christina Bartholdy1Janne Koch2Martin Fitzner Toft3Søren Skov4Camilla Hartmann Friis Hansen5Axel Kornerup Hansen6Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences University of Copenhagen Frederiksberg C DenmarkTranslational Sciences, Research & Early Development, LEO Pharma A/S Ballerup DenmarkTranslational Sciences, Research & Early Development, LEO Pharma A/S Ballerup DenmarkQM Diagnostics Nijmegen The NetherlandsDepartment of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences University of Copenhagen Frederiksberg C DenmarkDepartment of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences University of Copenhagen Frederiksberg C DenmarkDepartment of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences University of Copenhagen Frederiksberg C DenmarkAbstract Laboratory mice live in specific pathogen‐free (SPF) conditions, resulting in an immature immune system comparable to that of newborns rather than adult humans or mice from pet shops. This condition may compromise their translational value. Reintroducing pathogens would lead to the uncontrolled spread of infections and associated diseases, so research facilities should seek safer alternatives. We immunized laboratory mice with a cocktail of pathogens, which were inactivated by ultraviolet irradiation and mixed with the adjuvant AddaVax. This immunization resulted in a higher percentage of CD8+ effector memory T cells compared to untreated mice, although the response was not as robust as in pet shop mice. In a model of skin inflammation, pre‐immunization led to an increased skin inflammatory response compared to non‐immunized mice. All immunized mice seroconverted to the pathogens in the mixture, while none of the non‐immunized mice housed together seroconverted to the pathogens applied to the pre‐immunized mice. In conclusion, pre‐immunization of mice impacts the immune system, which includes increasing the levels of CD8+ effector memory T cells.https://doi.org/10.1111/cts.13697
spellingShingle Caroline Falkenberg
Christina Bartholdy
Janne Koch
Martin Fitzner Toft
Søren Skov
Camilla Hartmann Friis Hansen
Axel Kornerup Hansen
Induction of CD8+ immune memory and enhanced inflammation in a skin inflammation model through pre‐immunization with inactivated pathogens
Clinical and Translational Science
title Induction of CD8+ immune memory and enhanced inflammation in a skin inflammation model through pre‐immunization with inactivated pathogens
title_full Induction of CD8+ immune memory and enhanced inflammation in a skin inflammation model through pre‐immunization with inactivated pathogens
title_fullStr Induction of CD8+ immune memory and enhanced inflammation in a skin inflammation model through pre‐immunization with inactivated pathogens
title_full_unstemmed Induction of CD8+ immune memory and enhanced inflammation in a skin inflammation model through pre‐immunization with inactivated pathogens
title_short Induction of CD8+ immune memory and enhanced inflammation in a skin inflammation model through pre‐immunization with inactivated pathogens
title_sort induction of cd8 immune memory and enhanced inflammation in a skin inflammation model through pre immunization with inactivated pathogens
url https://doi.org/10.1111/cts.13697
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