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Details

Autor(en) / Beteiligte
Titel
Adult Acute Lymphoblastic Leukemia Phenotypes Defined by Monoclonal Antibodies
Ist Teil von
  • Blood, 1985-03, Vol.65 (3), p.730-735
Ort / Verlag
Washington, DC: Elsevier Inc
Erscheinungsjahr
1985
Quelle
Electronic Journals Library
Beschreibungen/Notizen
  • Pretreatment peripheral blood and/or bone marrow blasts from 90 adults with acute lymphoblastic leukemia (ALL) were analyzed as part of a prospective treatment protocol study. Specimens were tested by immunofluorescence cytofluorometry for reactivity with the following monoclonal antibodies (MoAbs): BA-1 (B cell antigen); T101, OKT11 (pan-T cell antigens [T]); 3A1 (T cell antigen); MCS-2 (myeloid antigen); J5 common ALL antigen (CALLA); BA4 (Ia antigen [Ia]); BA-2 (lymphohematopoietic antigen). Four major phenotypic groups were identified: B lineage ALL (BA-1+ T ) (64%), T lineage ALL (T+ BA-1 MCS-2 ) (13%), unclassified ALL (BA-1 MCS-2 CALLA T−) (9%) and myeloid antigen ALL (MCS-2+ CALLA T−) (7%). An additional group of patients, miscellaneous ALL (7%), was comprised of cases with unusual marker profiles. In B lineage ALL, all cases tested were Ia+ MCS-2−, and the vast majority were CALLA+ (84%). In T lineage ALL, 42% expressed CALLA or Ia positivity. In unclassified ALL, the predominant phenotype was Ia BA-2. In myeloid antigen ALL, two of four tested were 3A1+ and all cases evaluated were BA-1 . Patients with myeloid antigen ALL were older (median age, 66 years) than patients in the other groups. The T lineage ALL group had higher leukocyte counts (median WBCs, 183,000/μL) and an increased incidence of anterior mediastinal mass at presentation. All patients received identical induction therapy. In CALLA+ B lineage ALL, 30 of 46 (65%) achieved a complete remission. While the number of patients evaluated was small, 9 of 9 CALLA B-lineage ALL and only two of six myeloid antigen ALL cases responded with a complete remission. The data suggest that these MoAbs are useful in the characterization of adult ALL.
Sprache
Englisch
Identifikatoren
ISSN: 0006-4971
eISSN: 1528-0020
DOI: 10.1182/blood.V65.3.730.730
Titel-ID: cdi_proquest_miscellaneous_75981278

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