A Current Viewpoint of Lymphangioleiomyomatosis Supporting Immunotherapeutic Treatment Options

作者:Dilling Daniel F; Gilbert Emily R; Picken Maria M; Eby Jonathan M; Love Robert B; Le Poole I Caroline*
来源:American Journal of Respiratory Cell and Molecular Biology, 2012, 46(1): 1-5.
DOI:10.1165/rcmb.2011-0215TR

摘要

Lymphangioleiomyomatosis (LAM) leads to hyperproliferation of abnormal smooth muscle cells in the lungs, associated with diffuse pulmonary parenchymal cyst formation and progressive dyspnea on exertion. The disease targets women of child-bearing age. Complications include pneumothoraces and chylous pleural effusions. Ten-year survival is estimated at 70%, and lung transplantation remains the only validated treatment. It has been observed that LAM cells express markers associated with melanocytic differentiation, including gp100 and MART-1. Other melanocytic markers have also been observed. The same proteins are targeted by T cells infiltrating melanoma tumors as well as by T cells infiltrating autoimmune vitiligo skin, and these antigens are regarded as relatively immunogenic. Consequently, vaccines have been developed for melanoma targeting these and other immunogenic melanocyte differentiation proteins. Preliminary data showing susceptibility of LAM cells to melanoma-derived T cells suggest that vaccines targeting melanosomal antigens can be successful in treating LAM.

  • 出版日期2012-1