Interferon Lambda Signaling Restrains Experimental Autoimmune Encephalomyelitis
IFN-λ is a type III interferon (IFN) with pleiotropic functions in modulating immune responses. To address its function in autoimmune neuroinflammation, we evaluated the development and progression of experimental autoimmune encephalitis (EAE) in IFNLR1<i> </i>KO<i> (Ifnlr1</i&g...
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MDPI AG
2024-02-01
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| Series: | Biomedicines |
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| Online Access: | https://www.mdpi.com/2227-9059/12/3/526 |
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| author | Mohammad Asif Sherwani Samuel J. Duesman Zdenek Hel Chander Raman Nabiha Yusuf |
| author_facet | Mohammad Asif Sherwani Samuel J. Duesman Zdenek Hel Chander Raman Nabiha Yusuf |
| author_sort | Mohammad Asif Sherwani |
| collection | DOAJ |
| description | IFN-λ is a type III interferon (IFN) with pleiotropic functions in modulating immune responses. To address its function in autoimmune neuroinflammation, we evaluated the development and progression of experimental autoimmune encephalitis (EAE) in IFNLR1<i> </i>KO<i> (Ifnlr1</i><sup>−/−</sup><i>) </i>and C57Bl/6 (WT) mice following immunization with MOG<sub>3</sub><sub>5–55</sub> peptide. The results show that <i>Ifnlr1</i><sup>−/−</sup><i> </i>mice developed significantly more severe EAE than WT littermates with a similar day of onset, suggesting the potential of IFN-λ in reducing disease severity. We next interrogated whether IFN-λ differentially modulates EAE induced by encephalitogenic Th1 cells or Th17 cells. Encephalitogenic Th1 or Th17 generated from WT donors were transferred into WT or <i>Ifnlr1</i><sup>−/−</sup><i> </i>recipient mice. Whereas encephalitogenic Th1 cells induced more severe EAE in <i>Ifnlr1</i><sup>−/−</sup> than WT recipients, the disease severity induced by encephalitogenic Th17 cells was similar. Additionally, in vitro experiments showed that <i>Ifnlr1</i><sup>−/−</sup><i> </i>macrophages promoted the expansion of myelin peptide-reactive Th17 cells but not Th1 cells. Early in the disease, the spinal cords of EAE mice displayed a significantly greater proportion of Ly6C<sup>-</sup>Ly6G<sup>+</sup> cells with CXCR2<sup>+</sup>CD62L<sup>lo</sup> phenotype, indicating activated neutrophils. These findings suggest that IFN-λ signaling restrains activation and migration of neutrophils to the CNS, potentially attenuating neutrophil-mediated disease progression in autoimmune neuroinflammation. Recombinant IFN-λ can be used as a potential therapeutic target for treatment of patients with multiple sclerosis as it has fewer side effects due to the restricted expression of its receptor. |
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| format | Article |
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| institution | Directory Open Access Journal |
| issn | 2227-9059 |
| language | English |
| last_indexed | 2024-04-24T18:31:55Z |
| publishDate | 2024-02-01 |
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| series | Biomedicines |
| spelling | doaj.art-147fc30b1d9b43fd8a5e43122ec694b32024-03-27T13:22:41ZengMDPI AGBiomedicines2227-90592024-02-0112352610.3390/biomedicines12030526Interferon Lambda Signaling Restrains Experimental Autoimmune EncephalomyelitisMohammad Asif Sherwani0Samuel J. Duesman1Zdenek Hel2Chander Raman3Nabiha Yusuf4Department of Dermatology, University of Alabama at Birmingham, Birmingham, AL 35294, USADepartment of Dermatology, University of Alabama at Birmingham, Birmingham, AL 35294, USADepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294, USADepartment of Dermatology, University of Alabama at Birmingham, Birmingham, AL 35294, USADepartment of Dermatology, University of Alabama at Birmingham, Birmingham, AL 35294, USAIFN-λ is a type III interferon (IFN) with pleiotropic functions in modulating immune responses. To address its function in autoimmune neuroinflammation, we evaluated the development and progression of experimental autoimmune encephalitis (EAE) in IFNLR1<i> </i>KO<i> (Ifnlr1</i><sup>−/−</sup><i>) </i>and C57Bl/6 (WT) mice following immunization with MOG<sub>3</sub><sub>5–55</sub> peptide. The results show that <i>Ifnlr1</i><sup>−/−</sup><i> </i>mice developed significantly more severe EAE than WT littermates with a similar day of onset, suggesting the potential of IFN-λ in reducing disease severity. We next interrogated whether IFN-λ differentially modulates EAE induced by encephalitogenic Th1 cells or Th17 cells. Encephalitogenic Th1 or Th17 generated from WT donors were transferred into WT or <i>Ifnlr1</i><sup>−/−</sup><i> </i>recipient mice. Whereas encephalitogenic Th1 cells induced more severe EAE in <i>Ifnlr1</i><sup>−/−</sup> than WT recipients, the disease severity induced by encephalitogenic Th17 cells was similar. Additionally, in vitro experiments showed that <i>Ifnlr1</i><sup>−/−</sup><i> </i>macrophages promoted the expansion of myelin peptide-reactive Th17 cells but not Th1 cells. Early in the disease, the spinal cords of EAE mice displayed a significantly greater proportion of Ly6C<sup>-</sup>Ly6G<sup>+</sup> cells with CXCR2<sup>+</sup>CD62L<sup>lo</sup> phenotype, indicating activated neutrophils. These findings suggest that IFN-λ signaling restrains activation and migration of neutrophils to the CNS, potentially attenuating neutrophil-mediated disease progression in autoimmune neuroinflammation. Recombinant IFN-λ can be used as a potential therapeutic target for treatment of patients with multiple sclerosis as it has fewer side effects due to the restricted expression of its receptor.https://www.mdpi.com/2227-9059/12/3/526interferon lambdamultiple sclerosisneutrophils |
| spellingShingle | Mohammad Asif Sherwani Samuel J. Duesman Zdenek Hel Chander Raman Nabiha Yusuf Interferon Lambda Signaling Restrains Experimental Autoimmune Encephalomyelitis Biomedicines interferon lambda multiple sclerosis neutrophils |
| title | Interferon Lambda Signaling Restrains Experimental Autoimmune Encephalomyelitis |
| title_full | Interferon Lambda Signaling Restrains Experimental Autoimmune Encephalomyelitis |
| title_fullStr | Interferon Lambda Signaling Restrains Experimental Autoimmune Encephalomyelitis |
| title_full_unstemmed | Interferon Lambda Signaling Restrains Experimental Autoimmune Encephalomyelitis |
| title_short | Interferon Lambda Signaling Restrains Experimental Autoimmune Encephalomyelitis |
| title_sort | interferon lambda signaling restrains experimental autoimmune encephalomyelitis |
| topic | interferon lambda multiple sclerosis neutrophils |
| url | https://www.mdpi.com/2227-9059/12/3/526 |
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