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1. |
Requirements for growth of human erythroid progenitors in nutrient agar |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 207-217
E. Januszewicz,
I. A. Cooper,
T. R. Bradley,
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摘要:
AbstractHuman erythroid bursts and neutrophil colonies from fetal liver, term cord blood, and adult bone marrow were grown in nutrient agar, and the colonies were scored using a fixed whole plate method. Human placental conditioned medium was shown to contain burst promoting activity, and low oxygen tension markedly enhanced growth of erythroid bursts. Morphological analysis of colonies showed that eosinophil colonies were more numerous in bone marrow than fetal liver and conversely macrophage and neutrophil‐macrophage colonies were more numerous in fetal liver. Erythroid bursts were more numerous and larger in fetal liver. Human fetal liver cells do not produce endogenous colony‐stimulating fac
ISSN:0361-8609
DOI:10.1002/ajh.2830150302
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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2. |
Glycophorin a expression in malignant hematopoiesis |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 219-226
Kristof Liszka,
Otto Majdic,
Peter Bettelheim,
Walter Knapp,
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摘要:
AbstractTwo hundred twenty‐nine patients with hematopoietic malignancies were tested for reactivity with a monoclonal anti‐human glycophorin A antibody. One hundred twenty‐three of these cases were classified as acute leukemias of either the myeloid, lymphoid, erythroid, or undifferentiated type. The monoclonal antibody we used (VIE‐G4) was obtained after immunization with a human thymocyte suspension. It selectively reacts with glycophorin A (GpA) and strongly binds to 40% of K‐562 cells and all morphologically recognizable erythroid precursor cells. Apart from two cases with acute erythroid leukemia, this antibody reacted with none of the malignant cells in the 229 tested hematopoietic malignancies, including the 121 nonerythroid acute leukemias. This finding seems to contradict the earlier observations by L. Andersson and colleagues that a considerable proportion of acute leukemias express GpA on their surface. One reason for this discrepancy might be the fact that VIE‐G4 detects only complete glycosylated GpA. If this is the sole explanation, this would mean that the poorly differentiated cells in these cases express incompletely glyco
ISSN:0361-8609
DOI:10.1002/ajh.2830150303
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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3. |
The clonogenic assay as a reproducible in vitro system to study predictive parameters of treatment outcome in acute nonlymphoblastic leukemia |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 227-235
George Browman,
Jack Goldberg,
Arlan J. Gottlieb,
Harvey D. Preisler,
Nozar Azarnia,
Roger L. Priore,
James K. Brennan,
William R. Vogler,
Elliott F. Winton,
Kenneth B. Miller,
Hans Grunwald,
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摘要:
AbstractSeven institutions studied the cloning pattern of leukemic cells from pretherapy bone marrows of 273 patients with newly presenting and relapsed acute nonlymphoblastic leukemia. The cloning assay was done in all centers using an identical double‐layer agar method with a common source of colony‐stimulating factor. Cells were incubated for seven days, and clones were identified visually with an inverted microscope. All centers were able to obtain clonal growth in a substantial proportion of patients. Differences in growth pattern were observed between the major contributing center and the pooled results for all other centers. However, an analysis of clinical results suggested that in vitro differences were more likely related to differences in the patient populations than to variability in laboratory technique. The proportion of marrows in which leukemic cells formed colonies (>40 cells) and large clusters (20‐40 cells) was greater in relapsed patients than in newly presenting patients (P30% killing by in vitro drug exposure, and CR was obtained in only 30% of 23 patients whose marrows showed<30% killing (P<.01). The results indicate that the clonogenic assay correlates with treatment outcome and can be used for drug sensitivity testing in patients with acute nonlymphoblastic leukemia. The limitations of the assay are disc
ISSN:0361-8609
DOI:10.1002/ajh.2830150304
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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4. |
Ultrastructural studies of myeloma cells: Observations concerning the Golgi apparatus and intermediate‐size filaments |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 237-251
Margit Pavelka,
Heinz Ludwig,
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摘要:
AbstractStudies on the ultrastructure of tumor cells of 22 multiple myeloma patients revealed hitherto unreported observations concerning the Golgi apparatus and intermediate‐size filaments. Various abnormalities of the Golgi apparatus including displacements of the Golgi stacks, dilatations of cisternae, and massive accumulations of vesicles as well as vacuoles in the Golgi region were found in myeloma cells of 11 patients.Intermediate‐size filaments forming a fine intracytoplasmic network were apparent in myeloma cells of all 22 patients. In five patients, in addition to this architecture, intermediate‐size filaments were gathered into thick bundles which were primarily but not exclusively located in the perinuclear r
ISSN:0361-8609
DOI:10.1002/ajh.2830150305
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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5. |
Splenectomy for thrombocytopenia in chronic lymphocytic leukemia |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 253-259
Stuart A. Merl,
Michael E. Theodorakis,
Jack Goldberg,
Arlan J. Gottlieb,
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摘要:
AbstractThe role of peripheral platelet destruction as a reversible etiology of thrombocytopenia in chronic lymphocytic leukemia (CLL) was evaluated in nine patients with CLL and refractory thrombocytopenia who underwent splenectomy. The patients' ages ranged from 54 to 74 years. Progressive thrombocytopenia refractory to antineoplastic agents and corticosteroids had been present for a mean of 23.4 months. The platelet counts were 4,000–57,000/μl, and were generally higher in those patients with larger spleens. The spleens ranged from 180 to 4050 gm.Seven patients responded completely to splenectomy, achieving platelet counts>150,000/μl, and in one other patient, the count rose to>100,000/μl. The platelet count of one patient failed to respond to surgery. Those patients with massive splenomegaly developed higher, more rapidly rising platelet counts postoperatively. No operative mortality was encountered. Median hospitalization was seven postoperative days. All patients experienced an increased sense of well‐being. Median follow‐up time is
ISSN:0361-8609
DOI:10.1002/ajh.2830150306
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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6. |
A rapid in vitro drug‐sensitivity assay in acute nonlymphocytic leukemia |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 261-271
Michael E. Theodorakis,
Jack Goldberg,
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摘要:
AbstractLeukemic myeloid, myelomonocytic, and monocytic cells will incorporate radiolabeled sulfate into newly synthesized macromolecules. We developed a liquid culture technique to examine the in vitro effects of chemotherapeutic agents on the incorporation of radiolabeled sulfate into cells of patients with acute nonlymphocytic leukemia (ANLL). Cells recovered from bone marrow or peripheral blood of 25 patients with ANLL were incubated in vitro for one hour with saline (control) or a variety of chemotherapeutic agents. Cells were washed free of the drug and grown in liquid cultures containing nutrient medium and35SO4. The percent of35SO4incorporated into the drug treated as compared with control cells was determined after one, three, and seven days of culture. Patients whose drug‐treated cells incorporated less than 30% of35SO4when compared with the control after three or seven days of culture achieved a complete response to these agents in vivo (P<.05). Thus, the in vitro effects of various chemotherapeutic agents on the incorporation of35SO4into cells obtained from patients with ANLL may help predict clinical response to these agents in viv
ISSN:0361-8609
DOI:10.1002/ajh.2830150307
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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7. |
Intracranial myeloid metaplasia: Diagnosis by CT and Fe52scans and treatment by cranial irradiation |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 273-278
Dennis B. Cornfield,
Paul Shipkin,
Abass Alavi,
Joseph Becker,
Robert Peyster,
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摘要:
AbstractA patient with longstanding agnogenic myeloid metaplasia developed a progressive dementia. CT scanning demonstrated multiple intracranial masses, and a Fe52bone marrow scan demonstrated erythroid activity within the masses and confirmed the suspicion of extramedullary hematopoiesis. A potentially hazardous biopsy was avoided, and a course of cranial irradiation was administered, resulting in regression of the masses and clearing of the patient's dementia. Fe52scintigraphy provides a specific and useful diagnostic approach which may eliminate the need for invasive procedures.
ISSN:0361-8609
DOI:10.1002/ajh.2830150308
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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8. |
Inhibition of cold insolubility of an IgA cryoglobulin by decanedicarboxylic acid and related compounds |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 279-288
Parviz Lalezari,
Mahendra Kumar,
Kalpana M. Kumar,
Christine Lawrence,
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摘要:
AbstractCold insolubility of a serum IgA cryoimmunoglobulin was found to be inhibited by the addition of 1.5 mM sodium decanedicarboxylate in vitro. The patient with the cryoglobulin had advanced multiple myeloma complicated by severe hyperviscosity that caused lethargy and episodic loss of consciousness. Decanedicarboxylic acid administered orally resulted in transient relief of symptoms and the loss of cryoprecipitability of the paraprotein. Further in vitro studies revealed that sodium salts of long‐chain monocarboxylic acids with a minimum of eight carbons, and dicarboxylic acids with a minimum of 12 carbons inhibited cryoprecipitation. Salts of short‐chain carboxylic acids, by contrast, enhanced cryoprecipitation. Sodium phenolate and sodium salts of benzoic acid, 2,4‐DNP, phenylpropionic acid, and salicylic acid were also inhibitory. These latter compounds, which have a ring structure, did not cause precipitation at any concentration. It was demonstrated that the presence of a free carboxylic group was required for these activities; conversion of carboxylic acid to amide resulted in the loss of both the inhibitory and cryoprecipitation‐enhancing effects. Normal plasma, or plasma from five other patients who had IgG, IgM, or mixed‐type cryoglobulinemia, were not affected by any of these compounds. It is suggested that in selected cases of hyperviscosity syndrome associated with cryoglobulinemia, some of these compounds, especially monocarboxylic acids with appropriate chain lengths, or those with a ring structure, may have therapeutic app
ISSN:0361-8609
DOI:10.1002/ajh.2830150309
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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9. |
Chronic myelomonocytic leukemia with a chromosome abnormality (46,XY,20q–) in all dividing myeloid cells: Evidence for clonal origin in a multipotent stem cell common to granulocyte, monocyte, erythrocyte, and thrombocyte |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 289-293
Tamiko Shinohara,
Noriko Takuwa,
Kazuhiro Morishita,
Ryuji Ieki,
Jun Yokota,
Emiko Nakayama,
Shigetaka Asano,
Shiro Miwa,
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摘要:
AbstractIn a typical case of chronic myelomonocytic leukemia (CMML), a chromosome abnormality, 46, XY,20q‐, was observed in all the dividing cells including up to 16‐ploid cells in the bone marrow and the blood. As the mitotic figures could be easily seen not only in myelomonocytoid cells but also in erythroblasts in the bone marrow smear, it was concluded that all the cell lineages except lymphocytes had the abnormality. The present case will support the view that the leukemic process in CMML affects a multipotent stem cell rather than a granulocyte‐monocyte committed stem
ISSN:0361-8609
DOI:10.1002/ajh.2830150310
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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10. |
Acquired partial deletions of the long arm of chromosome 5 in hematologic disorders |
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American Journal of Hematology,
Volume 15,
Issue 3,
1983,
Page 295-310
Lawrence P. Wisniewski,
Kurt Hirschhorn,
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摘要:
AbstractWe have analyzed the data on 105 patients reported with a deletion of part of the long arm of chromosome 5 in the presence of hematologic disease. The major conditions associated with this abnormality are refractory anemia, polycythemia vera, and acute myelogenous leukemia, as well as the occasional occurrence of several other problems.
ISSN:0361-8609
DOI:10.1002/ajh.2830150311
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1983
数据来源: WILEY
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