1991
DOI: 10.1097/00007890-199102000-00032
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Cytomegalovirus Serologic Status and Postoperative Infection Correlated With Risk of Developing Chronic Rejection After Pulmonary Transplantation

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Cited by 192 publications
(66 citation statements)
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“…Additional associated risk factors include viral infection [29,31,32,[56][57][58][59][60][61][62][63][64], bacterial infection [65][66][67][68] and fungal infection [69][70][71]. Cytomegalovirus infection engages both the innate and adaptive components of immunity and causes upregulation of HLA class I and class II antigens on epithelial cells [72,73], and stimulates and augments the generation of allogeneic immune responses and proinflammatory cytokines [72,74].…”
Section: Other Risk Factorsmentioning
confidence: 99%
“…Additional associated risk factors include viral infection [29,31,32,[56][57][58][59][60][61][62][63][64], bacterial infection [65][66][67][68] and fungal infection [69][70][71]. Cytomegalovirus infection engages both the innate and adaptive components of immunity and causes upregulation of HLA class I and class II antigens on epithelial cells [72,73], and stimulates and augments the generation of allogeneic immune responses and proinflammatory cytokines [72,74].…”
Section: Other Risk Factorsmentioning
confidence: 99%
“…К дополни тельным факторам риска относятся вирусные [29,31,32,[56][57][58][59][60][61][62][63][64], бактериальные [65][66][67][68] и грибковые инфекции [69][70][71]. Цитомегаловирусной инфекцией поражаются как врожденный, так и адаптивный компоненты иммунитета и стимулируется выработ ка антигенов HLA I и II классов на эпителиальных клетках [72,73], а также стимулируется и усиливает ся аллогенный иммунный ответ и синтез провоспа лительных цитокинов [72,74].…”
Section: рекомендацияunclassified
“…In addition to alloimmune and/ or autoimmune phenomena associated with BOS, many mechanisms that can be perceived as predominantly nonimmune have been implicated as playing a role in BOS pathogenesis. These include injury caused by primary graft dysfunction (PGD) [36,37], gastroesophageal reflux (GER) with microaspiration [38,39], airway ischemia caused by disruption of the bronchial circulation [40•], and infections caused by viruses [41,42], bacteria [43,44], or fungi [45]. These "non-immune" factors may promote tissue inflammation that in turn initiates and may intensify an alloimmune rejection response or autoimmune reaction to lung airway self-antigens.…”
Section: Pathogenesis and Mechanisms Of Obliterative Bronchiolitismentioning
confidence: 99%