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11. |
Detection of Cystic Fibrosis Protein by Electrofocusing |
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Pediatric Research,
Volume 10,
Issue 12,
1976,
Page 1001-1002
GREGORY WILSON,
PHILIPPE ARNAUD,
MELVIN MONSHER,
H. FUDENBERG,
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PDF (275KB)
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ISSN:0031-3998
出版商:OVID
年代:1976
数据来源: OVID
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12. |
Severe Combined Immunodeficiency with Cartilage‐Hair HypoplasiaIn VitroResponse to Thymosin and Attempted Reconstitution |
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Pediatric Research,
Volume 10,
Issue 12,
1976,
Page 1003-1006
RUSSELL STEELE,
HOWARD BRITTON,
CLAUDE ANDERSON,
WILLIAM KNIKER,
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摘要:
ExtractThe present report describes an infant with severe combined immunodeficiency and cartilage-hair hypoplasia whose lymphocytes responded to thymosinin vitro.Immunologic evaluation was undertaken at 4 1/2 months of age following a history of recurrent severe infection. Family history included three cousins who died in early infancy, one from streptococcal meningitis and pneumonia, one from generalized varicella, and another from reticuloendotheliosis.Quantitative immunoglobulins were markedly depressed: IgG 141, IgA 0, and IgM 24 mg/100 ml. There was an absolute lymphopenia, multiple skin tests were negative, andin vitrolymphocyte responses to mitogens and antigens were depressed. Spontaneous E rosette determinations were 21% compared with control values of 65.7%. Erythrocyte adenosine deaminase (ADA) activity was normal.The patient's E rosette formation increased in the presence of thymosin, fraction 5, reaching a maximum of 56% with a concentration of 500 μg thymosin. Blastogenic responses to phytohemag-glutinin also increased in the presence of thymosin. Transplantation of 24-week fetal thymus in Millipore diffusion chambers and subsequently transplantation of 18-week fetal thymus by intra-peritoneal injection was accomplished. E rosettes increased to 35–40% and blastogenic responses to mitogens increased. Eight days after the second transplant the patient underwent a mild graft vs. host reaction which subsided after 1 week and mitogen blastogenic responses again increased to 5–8 times previous values, but still well below control ranges. Repeated episodes of pulmonary infection ensued, cor pulmonale resulted, and the clinical course was relentlessly downhill with the patient expiring from respiratory failure 5 months after transplantation.SpeculationReconstitution for primary cellular immune deficiency requires two steps:(1)provision of an adequate population of precursor lymphoid tissue which engrafts into the host and(2)maturation of available and/or transplanted cells. Some patients only require therapy directed toward the latter process and this can be accomplished with thymosin, transfer factor, fetal thymus in a diffusion chamber, or with fetal thymus by injection or transplant. Other patients, however, require transplantation of precursor lymphoid tissue, usually from bone marrow. Response to thymosinin vitrowill not accurately separate these two groups of patients.
ISSN:0031-3998
出版商:OVID
年代:1976
数据来源: OVID
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13. |
Index to Volume 10 |
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Pediatric Research,
Volume 10,
Issue 12,
1976,
Page 1007-1007
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PDF (530KB)
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ISSN:0031-3998
出版商:OVID
年代:1976
数据来源: OVID
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