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A host\u2019s tolerance may be improved by modulating the immune system such that it responds more rapidly and robustly in all facets, ranging from the recognition of pathogens to their clearance from the host. An understanding of biological processes and genes that are perturbed during attempted fungal exposure, colonization, and\/or invasion will help guide the identification of endogenous immunomodulators and\/or small molecules that activate host-immune responses such as specialized adjuvants.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>In this study, we present computational techniques and approaches using publicly available transcriptional data sets, to predict immunomodulators that may act against multiple fungal pathogens. Our study analyzed data sets derived from host cells exposed to five fungal pathogens, namely,<jats:italic>Alternaria alternata<\/jats:italic>,<jats:italic>Aspergillus fumigatus<\/jats:italic>,<jats:italic>Candida albicans<\/jats:italic>,<jats:italic>Pneumocystis jirovecii<\/jats:italic>, and<jats:italic>Stachybotrys chartarum<\/jats:italic>. We observed statistically significant associations between host responses to<jats:italic>A. fumigatus<\/jats:italic>and<jats:italic>C. albicans<\/jats:italic>. Our analysis identified biological processes that were consistently perturbed by these two pathogens. These processes contained both immune response-inducing genes such as MALT1, SERPINE1, ICAM1, and IL8, and immune response-repressing genes such as DUSP8, DUSP6, and SPRED2. We hypothesize that these genes belong to a pool of common immunomodulators that can potentially be activated or suppressed (agonized or antagonized) in order to render the host more tolerant to infections caused by<jats:italic>A. fumigatus<\/jats:italic>and<jats:italic>C. albicans<\/jats:italic>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Our computational approaches and methodologies described here can now be applied to newly generated or expanded data sets for further elucidation of additional drug targets. Moreover, identified immunomodulators may be used to generate experimentally testable hypotheses that could help in the discovery of broad-spectrum immunotherapeutic interventions. All of our results are available at the following supplementary website:<jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"http:\/\/bioinformatics.cs.vt.edu\/~murali\/supplements\/2013-kidane-bmc\" ext-link-type=\"uri\">http:\/\/bioinformatics.cs.vt.edu\/~murali\/supplements\/2013-kidane-bmc<\/jats:ext-link><\/jats:p><\/jats:sec>","DOI":"10.1186\/1471-2180-13-224","type":"journal-article","created":{"date-parts":[[2013,10,7]],"date-time":"2013-10-07T13:05:06Z","timestamp":1381151106000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["Computational approaches for discovery of common immunomodulators in fungal infections: towards broad-spectrum immunotherapeutic interventions"],"prefix":"10.1186","volume":"13","author":[{"given":"Yared H","family":"Kidane","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christopher","family":"Lawrence","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T M","family":"Murali","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2013,10,7]]},"reference":[{"issue":"12","key":"2476_CR1","doi-asserted-by":"publisher","first-page":"1842","DOI":"10.3201\/eid1112.050997","volume":"11","author":"ME Woolhouse","year":"2005","unstructured":"Woolhouse ME, Gowtage-Sequeria S: Host range and emerging and reemerging pathogens. 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