国际免疫学杂志
國際免疫學雜誌
국제면역학잡지
INTERNATIONAL JOURNAL OF IMMUNOLOGY
2011年
3期
204-208
,共5页
恶性黑色素瘤%肿瘤浸润淋巴细胞%抗细胞毒性T细胞相关抗原4抗体%BRAF阻断剂
噁性黑色素瘤%腫瘤浸潤淋巴細胞%抗細胞毒性T細胞相關抗原4抗體%BRAF阻斷劑
악성흑색소류%종류침윤림파세포%항세포독성T세포상관항원4항체%BRAF조단제
Malignant melanoma%Tumor infiltrating lymphocytes%Anti-CTLA-4 monoclonal antibody%Inhibition of BRAF
恶性黑色素瘤是一种恶性程度极高的皮肤肿瘤,病人发生转移后应用传统治疗方法很难达到有效治疗.自从恶性黑色素瘤的肿瘤抗原表位被发现后,恶性黑色素瘤的免疫治疗就开始成为研究热点.过继性细胞治疗临床应用研究在近几年内得到快速发展,其中疗效最好的当属肿瘤浸润淋巴细胞(TIL)回输治疗,其治疗有效率可以达到70%以上.同时,各种用于调节免疫系统的单克隆抗体药物以及信号传导阻滞剂的研究也在快速发展,这些研究为恶性黑色素瘤的免疫治疗提供了新思路.多种不同作用机制的药物疗效将在不久的将来得到证实,尤其是抗细胞毒性T细胞相关抗原4(CTLA-4)抗体的ipilimumab以及高选择性B型有丝分裂原激活的蛋白激酶依粘性激酶的激酶(BRAF)阻断剂PLX4032.
噁性黑色素瘤是一種噁性程度極高的皮膚腫瘤,病人髮生轉移後應用傳統治療方法很難達到有效治療.自從噁性黑色素瘤的腫瘤抗原錶位被髮現後,噁性黑色素瘤的免疫治療就開始成為研究熱點.過繼性細胞治療臨床應用研究在近幾年內得到快速髮展,其中療效最好的噹屬腫瘤浸潤淋巴細胞(TIL)迴輸治療,其治療有效率可以達到70%以上.同時,各種用于調節免疫繫統的單剋隆抗體藥物以及信號傳導阻滯劑的研究也在快速髮展,這些研究為噁性黑色素瘤的免疫治療提供瞭新思路.多種不同作用機製的藥物療效將在不久的將來得到證實,尤其是抗細胞毒性T細胞相關抗原4(CTLA-4)抗體的ipilimumab以及高選擇性B型有絲分裂原激活的蛋白激酶依粘性激酶的激酶(BRAF)阻斷劑PLX4032.
악성흑색소류시일충악성정도겁고적피부종류,병인발생전이후응용전통치료방법흔난체도유효치료.자종악성흑색소류적종류항원표위피발현후,악성흑색소류적면역치료취개시성위연구열점.과계성세포치료림상응용연구재근궤년내득도쾌속발전,기중료효최호적당속종류침윤림파세포(TIL)회수치료,기치료유효솔가이체도70%이상.동시,각충용우조절면역계통적단극륭항체약물이급신호전도조체제적연구야재쾌속발전,저사연구위악성흑색소류적면역치료제공료신사로.다충불동작용궤제적약물료효장재불구적장래득도증실,우기시항세포독성T세포상관항원4(CTLA-4)항체적ipilimumab이급고선택성B형유사분렬원격활적단백격매의점성격매적격매(BRAF)조단제PLX4032.
Melanoma is the most serious type of skin cancer and hard to be cured by traditional therapy when metastasis occurs in the patients. Since the immunogenicity of the melanoma was discovered,the biological and immune therapy for this tumour became a hot spot of research. The clinical research on adoptive cell transfer has developed rapidly in recent years and the most remarkable effecs obtained were the infusing of autotumor infiltrating lymphocyte with over a 70% partial response. In the mean time,the research on monoclonal antibodies and signalling pathway inhibitor has been progressing quickly. These researchs have provided new approaches to the biological and immune therapy. The effects of various medicine with different mechanisms will be demonstrated in the near future,especially ipilimumab,the anti-CTLA-4 monoclonal antibody and PLX4032,an highly selective inhibitor of BRAF.