4.6 Editorial Material

Anti-HER2/Neu passive-aggressive immunotherapy

期刊

ONCOIMMUNOLOGY
卷 3, 期 1, 页码 -

出版社

LANDES BIOSCIENCE
DOI: 10.4161/onci.27296

关键词

adaptive immunity; CD4; CD40; CD40L; CD8; HER2; Herceptin; antibody; immunotherapy; neu

资金

  1. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [T32AI007090] Funding Source: NIH RePORTER
  2. NCI NIH HHS [R01 CA141975, P01 CA097296] Funding Source: Medline
  3. NIAID NIH HHS [T32 AI007090] Funding Source: Medline

向作者/读者索取更多资源

Preclinical studies have established that CD8(+) T cells are necessary for efficient immunotherapeutic regimens targeting v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2 (ER BB2, best known as HER 2/Neu). Recently, we extended upon these findings by demonstrating that anti-HER 2/Neu therapy also requires CD4(+) T cells and CD40/CD40L signaling within the tumor microenvironment. Our results add to mounting evidence demonstrating that adaptive immunity is crucial to the efficacy of conventional and targeted anticancer chemotherapeutics.

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