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PMID: 2785753 Published · ppublish English Journal Article

Leu-22: a preferential marker for T-lymphocytes in paraffin sections. Staining profile in T- and B-cell lymphomas, Hodgkin's disease, other lymphoproliferative disorders, myeloproliferative diseases, and various neoplastic processes.

American journal of clinical pathology ·Vol. 91 ·No. 5 ·1989-05-00 ·Pages 542-9

Said JW, Stoll PN, Shintaku P, Bindl JM, Butmarc JR, Pinkus GS

Abstract

Monoclonal antibody Leu-22 represents an effective reagent for detection of neoplastic and nonneoplastic T-cells in paraffin sections of routinely processed tissues (242 specimens evaluated). In nonneoplastic tissues, immunoreactivity was localized mainly to lymphoid cells corresponding to a T-cell distribution. Immunoreactivity in lymphoid neoplasms, however, was preferentially, but not exclusively, limited to T-cell populations. Fifty-four of 60 T-cell neoplasms (90%) of various histologic types were Leu-22 positive. The pattern of immunoreactivity consisted mainly of membrane staining, with focal weak cytoplasmic positivity. Twenty-five of 67 B-cell neoplasms (37%) were also Leu-22 positive, with low-grade lymphomas (well/moderately well-differentiated lymphocytic types) representing most immunoreactive cases. In Hodgkin's disease, although most small lymphoid cells were Leu-22 positive, only rare Reed-Sternberg cells were immunoreactive. In all cases, histiocytes and myeloid cells exhibited variable immunoreactivity. The epitope identified by Leu-22 was detectable in formalin- and B5-fixed tissues but apparently was denatured after fixation in Zenker's-acetic acid solution used for bone marrow biopsies. Evaluation of a wide variety of nonhematopoietic neoplasms (64 total) revealed diffuse cytoplasmic staining in a few cases. However, membrane staining, typically noted for lymphoid cells, was not observed. Leu-22 potentially represents a useful marker for lymphoid cells, preferentially of T-cell origin, with optimal applicability as part of a panel that includes an effective pan-B-cell marker.

MeSH Terms
Antibodies, Monoclonal/immunology,metabolism B-Lymphocytes/immunology,metabolism,pathology Biomarkers, Tumor/immunology Cell Transformation, Neoplastic/immunology,pathology Hodgkin Disease/metabolism,pathology Humans Immunohistochemistry Lymphoma/immunology,metabolism,pathology Lymphoma, Non-Hodgkin/immunology,metabolism,pathology Lymphoproliferative Disorders/metabolism,pathology Myeloproliferative Disorders/metabolism,pathology Paraffin T-Lymphocytes/immunology,metabolism,pathology
Chemicals
Antibodies, Monoclonal Biomarkers, Tumor Paraffin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Said J W
Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, California.
Stoll P N
Shintaku P
Bindl J M
Butmarc J R
Pinkus G S
Article Info
Journal
American journal of clinical pathology
Abbr.
Am J Clin Pathol
ISSN
0002-9173
Published
1989-05-00
Pages
542-9
Language
English
Region
England
NLM ID
0370470
Subset
IM
Corrections
CommentIn
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