发明名称 Compositions Comprising Soluble HLA/M. Tuberculosis-Specific Ligand Complexes and Methods of Production and Use Thereof
摘要 Compositions that include at least one isolated, class I HLA trimolecular complex that includes a peptide ligand unique to M. tuberculosis-infected cells are disclosed. Isolated compositions that include the three components of the trimolecular complex and/or a polynucleotide encoding one or more of the three components are also disclosed.
申请公布号 US2015273039(A1) 申请公布日期 2015.10.01
申请号 US201514671322 申请日期 2015.03.27
申请人 THE BOARD OF REGENTS OF THE UNIVERSITY OF OKLAHOMA 发明人 Hildebrand William H.;McMurtrey Curtis;Lewinsohn David;Lewinsohn Deborah;Harriff Melanie
分类号 A61K39/04;G01N33/569 主分类号 A61K39/04
代理机构 代理人
主权项 1. A composition, comprising at least one of: (a) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:1, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (b) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:2 and/or 3, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (c) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:4, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (d) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:5, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (e) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising at least one of SEQ ID NOS:6-9, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (f) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:10 and/or 11, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (g) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:12 and/or 13, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (h) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:14, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (i) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:15, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (j) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:16, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (k) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising at least one of SEQ ID NOS:17-20, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (l) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:21, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (m) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:22, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (n) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:23 and/or 24, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (o) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:25 and/or 26, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (p) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:27, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; (q) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:28, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain; and (r) an isolated class I HLA trimolecular complex formed in vitro, the trimolecular complex comprising a soluble, truncated HLA-E heavy chain, beta-2-microglobulin, and a peptide comprising SEQ ID NO:29, and wherein the soluble, truncated HLA-E heavy chain does not contain the transmembrane and cytoplasmic domains of the native, full length HLA-E heavy chain.
地址 NORMAN OK US
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