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As increased numbers of memory CD8\n                    <jats:sup>+<\/jats:sup>\n                    T cells strongly correlate with enhanced protection against tumors and pathogenic infections, our findings identify the\n                    <jats:italic>Spry1<\/jats:italic>\n                    and\n                    <jats:italic>Spry2<\/jats:italic>\n                    loci as attractive targets for increasing the number, survival, and function of antigen-specific memory CD8\n                    <jats:sup>+<\/jats:sup>\n                    T cells. This may provide an opportunity for better future engineering of T cells against tumors and chronic viral infections.\n                  <\/jats:p>","DOI":"10.1073\/pnas.1808320115","type":"journal-article","created":{"date-parts":[[2018,8,20]],"date-time":"2018-08-20T15:15:20Z","timestamp":1534778120000},"update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":32,"title":["Lack of Sprouty 1 and 2 enhances survival of effector CD8\n                    <sup>+<\/sup>\n                    T cells and yields more protective memory cells"],"prefix":"10.1073","volume":"115","author":[{"given":"Hesham M.","family":"Shehata","sequence":"first","affiliation":[{"name":"Virology and Immunology, Gladstone Institutes, San Francisco, CA 94158;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shahzada","family":"Khan","sequence":"additional","affiliation":[{"name":"Virology and Immunology, Gladstone Institutes, San Francisco, CA 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