New England Journal of Medicine · 1982 · 990 citations · 15 references
ImmunohematologyImmunologyPathologyImmunodominanceImmunophenotypingImmunotherapeuticsLymphoma CloneImmunotherapyTumor BiologyTumor ImmunologyHematologyTumor ImmunitySurface MarkersAntibody EngineeringHealth SciencesB-cell LymphomaLymphoid NeoplasiaImmune SurveillanceAutoimmunityHumoral ImmunitySurface ImmunoglobulinAntibody ScreeningAntibody BiologyMedicine
Human B‑cell lymphomas arise from clonal proliferation of cells expressing a unique monoclonal surface immunoglobulin, whose variable region (idiotype) serves as a tumor‑specific marker distinguishing malignant from normal B cells. Anti‑idiotype antibodies have been shown to monitor B‑cell tumors and to investigate their biology. No additional information is provided.
HUMAN B-cell malignant tumors result from the proliferation of single clones of cells that express surface markers characteristic of normal B lymphocytes.1 , 2 In particular, the surface immunoglobulin expressed by these cells is monoclonal — i.e., restricted to a single light-chain type and to a particular variable region unique to each case. The unique immunoglobulin variable region (idiotype) of each lymphoma clone may be considered a tumor-specific marker, distinguishing tumor cells from normal cells in the patient. We and others have shown that anti-idiotype antibodies can be used to monitor B-cell tumors and to investigate the biology of these tumors.3 4 5 Because . . .
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Serotherapy of acute lymphoblastic leukemia with monoclonal antibody
J Ritz, JM Pesando, SE Sallan et al. · Blood · 1981 · 321 citations · Full text
The monoclonality of human B-cell lymphomas.
Ronald Levy, R Warnke, R. F. Dorfman et al. · The Journal of Experimental Medicine · 1977 · 267 citations · Full text