Volume 57, Issue S8 pp. 132-133
Article
Full Access

Reactivity of lung tumors with lung-derived and non-lung-derived monoclonal antibodies

H. L. Ioachim

Corresponding Author

H. L. Ioachim

Departments of Pathology of Lenox Hill Hospital and Cornell University Medical College, New York, NY, USA

Lenox Hill Hospital, 100 East 77 Street, New York, NY 10021, USASearch for more papers by this author
S. Pambuccian

S. Pambuccian

Departments of Pathology of Lenox Hill Hospital and Cornell University Medical College, New York, NY, USA

Search for more papers by this author
F. Giancotti

F. Giancotti

Departments of Pathology of Lenox Hill Hospital and Cornell University Medical College, New York, NY, USA

Search for more papers by this author
B. Dorsett

B. Dorsett

Departments of Pathology of Lenox Hill Hospital and Cornell University Medical College, New York, NY, USA

Search for more papers by this author
First published: 1994
Citations: 7

Abstract

The reactivity of 74 lung-derived monoclonal antibodies (MAbs) provided by the Third International Workshop on Lung Tumor Antigens and of 41 non-lung-derived commercially available MAbs against sections of 15 lung tumors of various histologic types was investigated by immunohistochemistry. Three MAbs with specificity for human neural-cell adhesion molecule (H-NCAM) and 3 MAbs with specificity for small-cell lung carcinoma (SCLC) were able to distinguish between neuroendocrine (NE) and non-NE tumors. Fifteen MAbs stained non-small-cell carcinomas (NSCLC) but not SCLC. Neuron-specific enolase (NSE) stained all NE tumors but also some of the non-NE tumors. Two MAbs showed specificity for mesotheliomas. Carcino-embryonic MAb strongly stained all SCLC and NSCLC. Among MAbs with lymphoid-cell specificities, Leu 7 (CD57) stained SCLC, but not NSCLC. LN2 (CD45R), LN3 (HLA-DR), Leu 22 (CD43) and BLA 36 reacted with NSCLC and were non-reactive with SCLC. Some of the lung-derived MAbs showed immune staining of lymphoma and melanoma.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.