{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T23:48:32Z","timestamp":1790380112379,"version":"4.1.0"},"reference-count":106,"publisher":"American Society of Hematology","issue":"9","content-domain":{"domain":["ashpublications.org"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2020,2,27]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Natural killer cell deficiencies (NKDs) are an emerging phenotypic subtype of primary immune deficiency. NK cells provide a defense against virally infected cells using a variety of cytotoxic mechanisms, and patients who have defective NK cell development or function can present with atypical, recurrent, or severe herpesviral infections. The current pipeline for investigating NKDs involves the acquisition and clinical assessment of patients with a suspected NKD followed by subsequent in silico, in vitro, and in vivo laboratory research. Evaluation involves initially quantifying NK cells and measuring NK cell cytotoxicity and expression of certain NK cell receptors involved in NK cell development and function. Subsequent studies using genomic methods to identify the potential causative variant are conducted along with variant impact testing to make genotype-phenotype connections. Identification of novel genes contributing to the NKD phenotype can also be facilitated by applying the expanding knowledge of NK cell biology. In this review, we discuss how NKDs that affect NK cell cytotoxicity can be approached in the clinic and laboratory for the discovery of novel gene variants.<\/jats:p>","DOI":"10.1182\/blood.2019000925","type":"journal-article","created":{"date-parts":[[2020,1,16]],"date-time":"2020-01-16T16:59:56Z","timestamp":1579193996000},"page":"629-637","update-policy":"https:\/\/doi.org\/10.1182\/blood.2019cm0000","source":"Crossref","is-referenced-by-count":8,"title":["A research-driven approach to the identification of novel natural killer cell deficiencies affecting cytotoxic function"],"prefix":"10.1182","volume":"135","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-9832-2395","authenticated-orcid":false,"given":"Michael T.","family":"Lam","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Columbia University Medical Center, New York, NY; and"},{"name":"Medical Scientist Training Program, and"},{"name":"Translational Biology and Molecular Medicine Graduate Program, 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