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suck abstract from ncbi


10.1159/000510251

http://scihub22266oqcxt.onion/10.1159/000510251
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32950975!?!32950975

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suck abstract from ncbi

pmid32950975      Pharmacology 2021 ; 106 (1-2): 9-19
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  • When Therapeutic IgA Antibodies Might Come of Age #MMPMID32950975
  • Sterlin D; Gorochov G
  • Pharmacology 2021[]; 106 (1-2): 9-19 PMID32950975show ga
  • BACKGROUND: Extensive efforts have been made in optimizing monoclonal immunoglobulin (Ig)G antibodies for use in clinical practice. Accumulating evidence suggests that IgA or anti-FcalphaRI could also represent an exciting avenue toward novel therapeutic strategies. SUMMARY: Here, we underline that IgA is more effective in recruiting neutrophils for tumor cell killing and is potently active against several pathogens, including rotavirus, poliovirus, influenza virus, and SARS-CoV-2. IgA could also be used to modulate excessive immune responses in inflammatory diseases. Furthermore, secretory IgA is emerging as a major regulator of gut microbiota, which impacts intestinal homeostasis and global health as well. As such, IgA could be used to promote a healthy microbiota in a therapeutic setting. Key messages: IgA combines multifaceted functions that can be desirable for immunotherapy.
  • |*COVID-19 Drug Treatment[MESH]
  • |*Immunotherapy/adverse effects[MESH]
  • |Animals[MESH]
  • |Anti-Inflammatory Agents/therapeutic use[MESH]
  • |Antibodies, Monoclonal/adverse effects/*therapeutic use[MESH]
  • |Antineoplastic Agents, Immunological/therapeutic use[MESH]
  • |Antiviral Agents/adverse effects/*therapeutic use[MESH]
  • |COVID-19/immunology/virology[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Immunoglobulin A/adverse effects/*therapeutic use[MESH]
  • |Inflammation/drug therapy/immunology[MESH]
  • |Mice[MESH]
  • |Neoplasms/drug therapy/immunology[MESH]


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