نتایج جستجو برای: leukocyte adhesion deficiency syndrome

تعداد نتایج: 840955  

Journal: :Journal of leukocyte biology 2004
Raffaele Badolato

The identification of chemokines has profoundly changed the way we interpret the immune response, elucidating the mechanism by which inflammatory cells are recruited to the site of infection by local secretion of chemoattractants such as CXC chemokine ligand 8 (CXCL8)/interleukin-8, chemokine ligand 2 (CCL2)/monocyte chemoattractant protein 1. This novel view of the immune response has been rem...

Journal: :Science translational medicine 2014
Niki M Moutsopoulos Joanne Konkel Mojgan Sarmadi Mehmet A Eskan Teresa Wild Nicolas Dutzan Loreto Abusleme Camille Zenobia Kavita B Hosur Toshiharu Abe Gulbu Uzel Wanjun Chen Triantafyllos Chavakis Steven M Holland George Hajishengallis

Leukocyte adhesion deficiency type I (LAD-I), a disease syndrome associated with frequent microbial infections, is caused by mutations on the CD18 subunit of β₂ integrins. LAD-I is invariably associated with severe periodontal bone loss, which historically has been attributed to the lack of neutrophil surveillance of the periodontal infection. We provide an alternative mechanism by showing that...

Journal: :Archives of Iranian medicine 2008
Reem Dababneh Adel M Al-Wahadneh Shamekh Hamadneh Antwan Khouri Nabil F Bissada

BACKGROUND Leukocyte adhesion deficiency type I (LAD-I) is an autosomal recessive immunodeficiency disorder characterized by defects in the integrin receptors of white blood cells that lead to impaired adhesion and chemotaxis. Affected patients are susceptible to recurrent bacterial and fungal infections, impaired pus formation, delayed wound healing, and periodontitis. METHODS A case of gene...

Journal: :American journal of clinical and experimental immunology 2014
Susanna C Fagerholm Hwee San Lek Vicky L Morrison

Kindlin-3 is a member of the kindlin family of focal adhesion proteins which bind to integrin beta-chain cytoplasmic domains to regulate integrin function. In contrast to kindlin-1 and kindlin-2 proteins, kindlin-3 is expressed mainly in the hematopoietic system. Mutations in kindlin-3 result in the rare genetic disorder, leukocyte adhesion deficiency type III (LAD-III), which is characterized ...

2011
Zeinab A El-Sayed Dalia H El-Ghoneimy Heba Abd-Allah Hanaa M Afifi

The β2 integrins are expressed exclusively on leukocytes and participate in many immune and inflammatory processes. This subfamily comprises four heterodimeric glycoproteins with a common β-subunit, designated β2 (CD18). Spontaneous mutations of the CD18 gene result in leukocyte adhesion deficiency type I (LAD-I). Low level of CD18 expression has also been implicated in the pathogenesis of psor...

Journal: :The Journal of clinical investigation 1999
N Hogg M P Stewart S L Scarth R Newton J M Shaw S K Law N Klein

In the leukocyte adhesion deficiency (LAD)-1 syndrome, there is diminished expression of beta2(CD18) integrins. This is caused by lesions in the beta2-subunit gene and gives rise to recurrent bacterial infections, impaired pus formation, and poor wound healing. We describe a patient with clinical features compatible with a moderately severe phenotype of LAD-1 but who expresses the beta2 integri...

Journal: :Journal of Veterinary Diagnostic Investigation 2013

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