2017
DOI: 10.1016/j.jim.2017.07.012
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An immunoproteomic approach revealed antigenic proteins enhancing serodiagnosis performance of bird fancier's lung

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Cited by 22 publications
(22 citation statements)
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“…7 from Fernández Pérez et al 10 ). 3,[41][42][43][44][45][46][47][48][49][50][51] We identified limitations of the diagnostic yield data from these studies including small samples, limited clinical context (eg, unclear exposure status, disease severity), inappropriate reference standards, test incorporation bias, and minimal reporting of testing information, and noted limitations to the use of serum antigen-specific tests including cross-reactivity among ubiquitous fungal species and avian antigens (increasing the risk of false-positive results), and poorly standardized techniques and antigen preparations (increasing the risk of false-negative results). 49,[52][53][54][55][56][57] We concluded there is insufficient evidence to support the use of serum antigen-specific antibody testing results to reliably confirm or rule out the diagnosis of HP in the absence of an identifiable IA or consistently identify the particular type of antigen (eg, mold) involved in the disease process.…”
Section: Fig 4 Fibrosismentioning
confidence: 99%
“…7 from Fernández Pérez et al 10 ). 3,[41][42][43][44][45][46][47][48][49][50][51] We identified limitations of the diagnostic yield data from these studies including small samples, limited clinical context (eg, unclear exposure status, disease severity), inappropriate reference standards, test incorporation bias, and minimal reporting of testing information, and noted limitations to the use of serum antigen-specific tests including cross-reactivity among ubiquitous fungal species and avian antigens (increasing the risk of false-positive results), and poorly standardized techniques and antigen preparations (increasing the risk of false-negative results). 49,[52][53][54][55][56][57] We concluded there is insufficient evidence to support the use of serum antigen-specific antibody testing results to reliably confirm or rule out the diagnosis of HP in the absence of an identifiable IA or consistently identify the particular type of antigen (eg, mold) involved in the disease process.…”
Section: Fig 4 Fibrosismentioning
confidence: 99%
“…Recombinant antigens are the most recent ones [43][44][45][46]58]. They are obtained after cloning a specific gene coding for a unique antigenic protein.…”
Section: Using Elisa Level Of Recombinant Antigens For Fld Bfl and Mwf-hpmentioning
confidence: 99%
“…However, these antigens correspond to a single protein and will thus reflect a limited part of the complex immunologic signals of the disease [43][44][45][46]58]. Numerous RAg were created, but only some of them were selected for three HP serodiagnoses: MWF-HP (Acyl-CoA-dehydrogenase (Acyl-CoA) and dihydrolipoyl dehydrogenase (DHDH)), FLD (SR17 hydroperoxidase (SR17) & Dihydrolipoamide dehydrogenase (DLDH)) and BFL (Immunoglobulin lamda-likepolypeptide-1 (IGLL1) and proproteinase E (ProE)) [43][44][45][46]. They can be used for ELISA (Enzyme Linked ImmunoSorbent Assay) with sensitivity and specificity reaching 80% and 90%, respectively, for MWF-HP [45], 83% and 77% for FLD [44] and 76% and 100% for BFL [46].…”
Section: Using Elisa Level Of Recombinant Antigens For Fld Bfl and Mwf-hpmentioning
confidence: 99%
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“…Our experience shows that some patients claim more than one exposure. It was found that at least some orthologous immunogenic proteins of inhalation antigens possess common epitopes (Rouzet et al, 2017); however, these epitopes have been described only in several antigens thus far. Currently, if EAA patients claim more potential sources of exposure, we are not sure whether all of them are clinically relevant and therefore should be avoided.…”
Section: Introductionmentioning
confidence: 99%