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Blood Adv ; 6(2): 399-404, 2022 01 25.
Artículo en Inglés | MEDLINE | ID: mdl-34559181

RESUMEN

Somatic mutations in JAK2, MPL and Calreticulin and inflammation play a key role in pathophysiology of chronic myeloproliferative neoplasia (CMN). One of the most prominent cytokines elevated in serum of Polycythemia vera patients is interleukin-6 (IL-6). Currently, it is being discussed whether suppression of inflammation by anti-cytokine approaches as anti-IL-6 treatment may be therapeutically useful in CMN. We here sought to investigate the efficacy of anti-IL-6 treatment on inflammatory cytokines, hematocrit and splenomegaly in CMN like disease. JAK2-V617F knock-in mice (JAK2+/V617F) were treated for three weeks with anti-IL-6 antibody (Ab) or IgG-control. Upon anti-IL-6 Ab treatment, serum levels of CXCL2 and CXCL10 were significantly reduced. In addition, CXCL1, CCL11, M-CSF, G-CSF, IL-17, IL-12p40 and CCL2 were reduced by a factor of 0.3 -- 0.8. Partly, this was also achieved by applying high-dose IgG. Hematocrit, erythrocyte and leukocyte counts were elevated in JAK2+/V617F mice but were not reduced by anti-IL6 Ab treatment. In addition, there was no apparent amelioration of splenomegaly and spleen histopathology. In conclusion, anti-IL-6 Ab treatment did not result in improvement of hematological disease parameters but was shown to modulate the serum cytokine signature.


Asunto(s)
Trastornos Mieloproliferativos , Policitemia Vera , Animales , Citocinas , Modelos Animales de Enfermedad , Hematócrito , Humanos , Inmunoglobulina G/uso terapéutico , Inflamación , Interleucina-6 , Ratones , Trastornos Mieloproliferativos/tratamiento farmacológico , Policitemia Vera/complicaciones , Policitemia Vera/tratamiento farmacológico , Policitemia Vera/genética , Esplenomegalia/tratamiento farmacológico , Esplenomegalia/etiología
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