ELISA based assays to measure adenosine deaminases concentration in serum and saliva for the diagnosis of ADA2 deficiency and cancer

dc.contributor.authorLuo Wenwen
dc.contributor.authorDong Liang
dc.contributor.authorChen Fenghong
dc.contributor.authorLei WenbinB
dc.contributor.authorHe Liya
dc.contributor.authorZhou Qing
dc.contributor.authorLamy Thierry
dc.contributor.authorZavialov Andrey V
dc.contributor.organizationfi=MediCity|en=MediCity|
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organization-code1.2.246.10.2458963.20.83772236069
dc.converis.publication-id176230785
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/176230785
dc.date.accessioned2025-08-27T21:32:21Z
dc.date.available2025-08-27T21:32:21Z
dc.description.abstractAdenosine deaminases (ADAs) are enzymes of purine metabolism converting adenosine to inosine. There are two types of ADAs in humans ADA1 and ADA2. While both ADA1 and ADA2 share the same substrate, they differ in expression, cellular localization, and catalytic properties. The genetic deficiency of ADA1 results in severe combined immunodeficiency (SCID), while lack in ADA2 (DADA2) results in multiple phenotypes ranging from systemic inflammation to vascular pathology. Clinical studies have shown that the levels of ADAs in biological fluids are altered in pathophysiological conditions, suggesting that ADA activity could be a convenient marker for the diagnosis of immune diseases and cancer. Here, we describe sensitive and straightforward ELISA assays to measure ADA1 and ADA2 concentrations in biological fluids. Analysis of the serum and saliva samples from the healthy controls and DADA2 patients revealed that ADA2 enzyme concentration is significantly lower in patients than in healthy controls. In contrast, the concentration of ADA2 increases in the serum of patients with large granular leukocyte leukemia (LGLL) and patients' saliva with head and neck cancer. Thus, this simple, non-invasive method allows for distinguishing healthy controls from the affected patient. It can be implemented in screening and diagnosis of DADA2 and follow up the treatment of LGLL and several types of head and neck cancer.
dc.identifier.olddbid200580
dc.identifier.oldhandle10024/183607
dc.identifier.urihttps://www.utupub.fi/handle/11111/45645
dc.identifier.urlhttps://doi.org/10.3389/fimmu.2022.928438
dc.identifier.urnURN:NBN:fi-fe2022091258474
dc.language.isoen
dc.okm.affiliatedauthorZavialov, Anton
dc.okm.affiliatedauthorDataimport, Biotekniikan keskuksen yhteiset
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherFrontiers Media SA
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.articlenumber928438
dc.relation.doi10.3389/fimmu.2022.928438
dc.relation.ispartofjournalFrontiers in immunology
dc.relation.volume13
dc.source.identifierhttps://www.utupub.fi/handle/10024/183607
dc.titleELISA based assays to measure adenosine deaminases concentration in serum and saliva for the diagnosis of ADA2 deficiency and cancer
dc.year.issued2022

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