Failure of IL-1 receptor antagonist and monoclonal anti-IL-1 receptor antibody to inhibit antigen-specific immune responses in vivo

rIL-1R antagonist (rIL-1ra) and 35F5, a neutralizing mAb, have been shown to inhibit the ability of IL-1 alpha and IL-1 beta to bind to type I but not type II murine receptors. Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we ha...

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Veröffentlicht in:The Journal of immunology (1950) 1992-02, Vol.148 (3), p.766-771
Hauptverfasser: Faherty, DA, Claudy, V, Plocinski, JM, Kaffka, K, Kilian, P, Thompson, RC, Benjamin, WR
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container_issue 3
container_start_page 766
container_title The Journal of immunology (1950)
container_volume 148
creator Faherty, DA
Claudy, V
Plocinski, JM
Kaffka, K
Kilian, P
Thompson, RC
Benjamin, WR
description rIL-1R antagonist (rIL-1ra) and 35F5, a neutralizing mAb, have been shown to inhibit the ability of IL-1 alpha and IL-1 beta to bind to type I but not type II murine receptors. Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we have evaluated the activity of human IL-1ra and 35F5 in murine Ag-specific cell-mediated and humoral immune response models. Administration of IL-1ra, either twice daily or as a continuous infusion, did not inhibit the cytolytic T lymphocyte response to allogeneic splenocytes. The CTL response was also not inhibited by daily administration of 35F5. The delayed type hypersensitivity response to oxazolone was similarly refractory to administration of IL-1ra and 35F5. In the humoral immune response models, neither the splenic plaque response to SRBC nor the IgG or IgM response to TNP-keyhole limpet hemocyanin was inhibited by treatment with IL-1ra or 35F5. These data suggest that signaling through the type I IL-1R is not required for these Ag-specific immune responses.
doi_str_mv 10.4049/jimmunol.148.3.766
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Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we have evaluated the activity of human IL-1ra and 35F5 in murine Ag-specific cell-mediated and humoral immune response models. Administration of IL-1ra, either twice daily or as a continuous infusion, did not inhibit the cytolytic T lymphocyte response to allogeneic splenocytes. The CTL response was also not inhibited by daily administration of 35F5. The delayed type hypersensitivity response to oxazolone was similarly refractory to administration of IL-1ra and 35F5. In the humoral immune response models, neither the splenic plaque response to SRBC nor the IgG or IgM response to TNP-keyhole limpet hemocyanin was inhibited by treatment with IL-1ra or 35F5. 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subjects Analysis of the immune response. Humoral and cellular immunity
Animals
Antibodies, Monoclonal
Antibody Formation - drug effects
Antigens - immunology
Biological and medical sciences
Cells, Cultured
Cytotoxicity, Immunologic - drug effects
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Immunobiology
In Vitro Techniques
Interleukin 1 Receptor Antagonist Protein
Interleukin-1 - pharmacology
Interleukin-6 - biosynthesis
Lymphokines, interleukins ( function, expression)
Mice
Mice, Inbred C57BL
Proteins - pharmacology
Receptors, Immunologic - physiology
Receptors, Interleukin-1
Regulatory factors and their cellular receptors
Sialoglycoproteins
T-Lymphocytes, Cytotoxic - immunology
title Failure of IL-1 receptor antagonist and monoclonal anti-IL-1 receptor antibody to inhibit antigen-specific immune responses in vivo
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