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  • Bone marrow transplantation  (2)
  • Opsonierung  (2)
  • chemotaxis  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 53 (1975), S. 643-652 
    ISSN: 1432-1440
    Keywords: Granulocytes ; function ; inborn defects ; chemotaxis ; opsonisation ; phagocytosis ; intracellular microbicidal activity ; Granulocyten ; Funktion ; angeborene Defekte ; Chemotaxis ; Opsonierung ; Phagocytose ; intracelluläre Keimabtötung
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die Funktion der Granulocyten und deren Störungen findet zunehmend Beachtung. Die vorliegende Übersicht soll den augenblicklichen Stand des Wissens zusammenfassen. Im ersten von zwei Teilen wird ein Überblick über die molekulare Basis der Granulocytenfunktion gegeben und die wesentlichsten angeborenen Störungen der Chemotaxis, Opsonierung, Phagocytose und intracellulären Abtötung von Keimen werden referiert.
    Notes: Summary The insight in the function and dysfunction of granulocytes lately arouses more and more interest. This report summarises our present knowledge. In the first of two chapters the authors review the molecular basis of granulocyte function and the inborn defects of chemotaxis, opsonisation, phagocytosis and intracellular killing of bacteria and fungi.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 53 (1975), S. 739-746 
    ISSN: 1432-1440
    Keywords: Granulocytes function ; secondary defects ; chemotaxis ; opsonisation ; phagocytosis ; intracellular microbicidal activity ; Granulocyten ; Funktion ; sekundäre Defekte ; Chemotaxis ; Opsonierung ; Phagocytose ; intrazelluläre Keimabtötung
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Im ersten Teil dieser Übersicht haben wir einen Überblick über die molekulare Basis der Granulocytenfunktion und deren wesentlichsten angeborenen Störungen gegeben. Der vorliegende zweite Teil soll das gegenwärtige Wissen über die sekundären Störungen der Chemotaxis, Opsonierung, Phagocytose und intracellulären Keimabtötung zusammenfassen.
    Notes: Summary In the first part we reviewed both the molecular basis of granulocyte function and the inborn defects. The present chapter summarizes our knowledge of the secondary defects of chemotaxis, opsonisation, phagocytosis and intracellular microbicidal activity.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1076
    Keywords: Severe combined immunodeficiency ; Bone marrow transplantation ; HLA-haploidentical donors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In 15 infants with severe combined immunodeficiency (SCID), immunological reconstitution was attempted by bone marrow transplantation (BMT) from HLA-haploidentical parents. To prevent graft versus host disease (GvHD), marrow grafts were depleted of contaminating T-lymphocytes using lectin agglutination and rosette formation with sheep red blood cells. Thirteen patients received transplants without undergoing prior cytoreductive conditioning. Eleven of these developed donor-dependent T-cell functions, two failed to do this. One of these two as well as two further patients received cytoreductive treatment prior to repeat and to first transplants and in two, complete lymphohemopoietic reconstitution was observed. Of the 15 patients who received transplants, 11 are currently alive. Two recently treated patients remain in the hospital, nine are at home with stable T-cell functions. Normal humoral immune functions have developed upto now in three patients. In the others, gammaglobulins are regularly substituted. Complications of acute or chronic GvHD were not observed with the exception of one case who developed transient GvHD of the skin. These results suggest that in a majority of patients with SCID, T-cell functions can develop without GvHD following haploidentical, T-cell-depleted BMT. Exceptional patients require preconditioning to allow donor cell engraftment, an approach that also appears to facilitate reconstitution of humoral immune functions
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1440
    Keywords: Bone marrow transplantation ; Aplastic anaemia ; Acute leukaemia ; Chronic granulocytic leukaemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary From 1972–1983 53 patients underwent bone marrow transplantation. The median age was 18 years (3–41). 27 patients suffered from severe aplastic anaemia, 22 patients had acute leukaemia and 4 patients had chronic granulocytic leukaemia in chronic phase. Out of 22 patients with acute leukaemia, 2 had florid leukaemia, 2 had an early relapse and 18 patients were in first or second remission of their disease. 2/53 patients received a syngeneic transplant, 51/53 patients an allogeneic transplant. 47/51 patients had a HLA-A, B, C-identical, MLC-negative sibling donor, 1/51 had a HLA-A, B-C-identical, MLC-positive sibling donor, 2/51 a HLA-phaenotypical identical parental donor and 1/51 a HLA-identical, MLC-negative unrelated donor. The comparison of the results obtained in patients with severe aplastic anaemia transplanted from 1972–1979 with those transplanted from 1980–1983 shows that the bone marrow transplantation has to be performed in an early stage of the disease before the patients become multiple transfused, sensitized and severely infected and that the conditioning regimen for polytransfused patients has to be more intensive than in untransfused patients. From the patient group transplanted 1972–1979, only 1/14 patients is a long-term survivor in contrast to 8/13 patients transplanted from 1980–1983. 11/22 patients with acute leukaemia are alive between more than 5 years and 14 days after bone marrow transplantation. Only 1/4 patients, who were transplanted not in remission, is alive. For patients with acute leukaemia the bone marrow transplantation should be performed in an early stage of their disease when the tumor burden is small and when the patients are in good clinical condition. 2/4 patients with CGL are alive between 12 months and 3 months after bone marrow transplantation. In our patient group graft versus host disease was the most important problem with a high mortality due to GvHD associated infections.
    Type of Medium: Electronic Resource
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