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PMID: 7687895 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Effect of Campath-1H antibody on human hematopoietic progenitors in vitro.

Blood ·Vol. 82 ·No. 3 ·1993-08-01 ·Pages 807-12

Gilleece MH, Dexter TM

Abstract

The humanized antibody CAMPATH-1H has been shown in pilot studies to be beneficial in the treatment of lymphoid malignancy and other lymphoproliferative diseases. The antigen recognized by this antibody is not confined to lymphoid cells, and work with rat antibodies of similar specificity has not eliminated the possibility of damage to human hematopoietic progenitors, particularly those capable of repopulating bone marrow and sustaining hematopoiesis. This study aimed to discover if hematopoietic progenitor cells were affected by treatment with CAMPATH-1H, with or without human complement. Bone marrow mononuclear cells from healthy volunteers were treated with saturating concentrations of CAMPATH-1H, human complement, or CAMPATH-1H plus human complement. The CD34-positive fraction of the mononuclear cells was treated similarly. Residual progenitor activity was measured in the colony-forming unit-granulocyte, erythroid, monocyte, megakaryocyte assay and compared with untreated controls. There was no significant difference (at the 5% level) between treated and control cells. Mononuclear cells were divided into CAMPATH-1H-positive and CAMPATH-1H-negative fractions by fluorescein isothiocyanate-CAMPATH-1H labeling and fluorescence-activated cell sorter separation. Hematopoietic progenitors were predominantly found in the CAMPATH-1H-negative fraction. Furthermore, mononuclear cells treated with CAMPATH-1H and complement were equivalent to controls in experiments that investigated the capacity of these cells to form hematopoietic foci in long-term cultures.

MeSH Terms
Antibody-Dependent Cell Cytotoxicity Antigens, CD/analysis,physiology Antigens, CD34 Antigens, Neoplasm Bone Marrow Cells CD52 Antigen Cell Separation Cells, Cultured Complement System Proteins/immunology Glycoproteins Hematopoiesis Hematopoietic Stem Cells/immunology Humans In Vitro Techniques Recombinant Fusion Proteins
Chemicals
Antigens, CD Antigens, CD34 Antigens, Neoplasm CD52 Antigen CD52 protein, human Cd52 protein, rat Glycoproteins Recombinant Fusion Proteins Complement System Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gilleece M H
Department of Experimental Haematology, CRC Paterson Institute for Cancer Research, Withington, Manchester, England.
Dexter T M
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1993-08-01
Pages
807-12
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
Wellcome Trust · United Kingdom
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