Compositions and methods related to antibodies that neutralize coagulase activity during
Embodiments concern methods and compositions for treating or preventing a bacterial infection, particularly infection by a Staphylococcus bacterium. Aspects include methods and compositions for providing a passive immune response against the bacteria, in certain embodiments, the methods and compositions involve an antibody that binds Coagulase (Coa).
1. A method of treating Staphylococcus infection in a patient determined to have or be at risk for Staphylococcus infection comprising administering to the patient an effective amount of a composition comprising a Coa binding antibody that specifically binds to Domains 1-2 or the repeat Domain of a Staphylococcal Coa polypeptide, wherein the Coa binding antibody comprises the sequence of the six CDR domains of a 7H4.25, 4H9.20, 4B10.44, 2A3.1, 2H10.12, 6D1.22, 6C4.15, 6C10.19, 8C2.9, or 4F1.7 monoclonal antibody,
wherein the 7H4.25 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSVDYNGISY (SEQ ID NO:9), AAS (SEQ ID NO:21), and HQSIEDPRT (SEQ ID NO:30) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFNIKDIY (SEQ ID NO:12), IDPADGHS (SEQ ID NO:31), and SRSGAI (SEQ ID NO:32),
wherein the 4H9.20 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSVDYNGISY (SEQ ID NO:9), AAS (SEQ ID NO:10), and QQSIEDPRT (SEQ ID NO:11) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFNIKDIY (SEQ ID NO:12), IDPANGNT (SEQ ID NO:13), and SRSGAY (SEQ ID NO:14),
wherein the 4B10.44 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSVDYNGISY (SEQ ID NO:9), AAS (SEQ ID NO:21), and HQSIEDPRT (SEQ ID NO:22) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFNIKDIY (SEQ ID NO:12), IDPANGNT (SEQ ID NO:13), and SRSGAF (SEQ ID NO:23),
wherein the 2A3.1 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRARKNY (SEQ ID NO:33), WAS (SEQ ID NO:34), and KQSYNLWT (SEQ ID NO:35) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of YTLTDYS (SEQ ID NO:37), INTETGEP (SEQ ID NO:38), and ARTARDY (SEQ ID NO:39),
wherein the 2H10.12 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRARKNY (SEQ ID NO:40), WAS (SEQ ID NO:34), and KQSYYLWT (SEQ ID NO:36) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GYTLTDYS (SEQ ID NO:41), INTETGEP (SEQ ID NO:38), and GRTARADY (SEQ ID NO:42),
wherein the 6D1.22 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRARKNY (SEQ ID NO:40), WAS (SEQ ID NO:34), and KQSYNLWT (SEQ ID NO:35) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GYTLTDYS (SEQ ID NO:41), INTETGDP (SEQ ID NO:43), and ARTARADY (SEQ ID NO:38),
wherein the 6C4.15 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRTRKIY (SEQ ID NO:44), WAS (SEQ ID NO:34), and KQSYYLYT (SEQ ID NO:45) and comprises a heavy chain CDR1, CDR2, and CDR3domain with the respective sequences of GFSFSNYW (SEQ ID NO:46), IRLKSDNYGT (SEQ ID NO:47), and SAYGDYEY (SEQ ID NO:48),
wherein the 6C10.19 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QNIVHSNGNTY (SEQ ID NO:56), KVS (SEQ ID NO:25), and LQGSNCSNH (SEQ ID NO:57) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GYEFTDFE (SEQ ID NO:50), FDPETGRS (SEQ ID NO:51), and SRFHYYGRTAY (SEQ ID NO:52),
wherein the 8C2.9 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRARKNY (SEQ ID NO:40), WAS (SEQ ID NO:34), and KQSYNLWT (SEQ ID NO:35) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFTFSNYY (SEQ ID NO:53), IKSNGVST (SEQ ID NO:54), and VRHDGYYFAY (SEQ ID NO:55), and
wherein the 4F1.7 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLFNSRARKNY (SEQ ID NO:49), WAS (SEQ ID NO:34), and KQSYNLWT (SEQ ID NO:35) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFSIKDTT (SEQ ID NO:58), IDPTDGHN (SEQ ID NO:59), and KQSYNLWT (SEQ ID NO:60).
2. The method of claim 1 , wherein the Coa binding antibody is a single chain antibody.
3. The method of claim 1 , wherein the Coa binding antibody is a recombinant fusion protein.
4. The method of claim 1 , wherein the Coa binding antibody comprises the sequence of the six CDR domains from the 7H4.25 monoclonal antibody.
5. The method of claim 1 , wherein the Coa binding antibody is a humanized or chimeric antibody.
6. The method of claim 1 , further comprising administering an antibiotic or a Staphylococcal vaccine composition.
7. A method of treating a patient having or at risk for Staphylococcus infection comprising administering to the patient an effective amount of a composition comprising a purified chimeric antibody comprising the sequence of the six CDR domains from a 7H4.25, 4H9.20, 4B10.44, 2A3.1, 2H10.12, 6D1.22, 6C4.15, 6C10.19, 8C2.9, or 4F1.7 monoclonal antibody,
wherein the 7H4.25 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSVDYNGISY (SEQ ID NO:9), AAS (SEQ ID NO:21), and HQSIEDPRT (SEQ ID NO:30) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFNIKDIY (SEQ ID NO:12), IDPADGHS (SEQ ID NO:31), and SRSGAI (SEQ ID NO:32),
wherein the 4H9.20 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSVDYNGISY (SEQ ID NO:9), AAS (SEQ ID NO:10), and QQSIEDPRT (SEQ ID NO:11) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFNIKDIY (SEQ ID NO:12), IDPANGNT (SEQ ID NO:13), and SRSGAY (SEQ ID NO:14),
wherein the 4B10.44 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSVDYNGISY (SEQ ID NO:9), AAS (SEQ ID NO:21), and HQSIEDPRT (SEQ ID NO:22) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFNIKDIY (SEQ ID NO:12), IDPANGNT (SEQ ID NO:13), and SRSGAF (SEQ ID NO:23),
wherein the 2A3.1 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRARKNY (SEQ ID NO:33), WAS (SEQ ID NO:34), and KQSYNLWT (SEQ ID NO:35) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of YTLTDYS (SEQ ID NO:37), INTETGEP (SEQ ID NO:38), and ARTARDY (SEQ ID NO:39),
wherein the 2H10.12 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRARKNY (SEQ ID NO:40), WAS (SEQ ID NO:34), and KQSYYLWT (SEQ ID NO:36) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GYTLTDYS (SEQ ID NO:41), INTETGEP (SEQ ID NO:38), and GRTARADY (SEQ ID NO:42),
wherein the 6D1.22 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRARKNY (SEQ ID NO:40), WAS (SEQ ID NO:34), and KQSYNLWT (SEQ ID NO:35) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GYTLTDYS (SEQ ID NO:41), INTETGDP (SEQ ID NO:43), and ARTARADY (SEQ ID NO:38),
wherein the 6C4.15 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3domain with the respective sequences of QSLLNSRTRKIY (SEQ ID NO:44), WAS (SEQ ID NO:34), and KQSYYLYT (SEQ ID NO:45) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFSFSNYW (SEQ ID NO:46), IRLKSDNYGT (SEQ ID NO:47), and SAYGDYEY (SEQ ID NO:48),
wherein the 6C10.19 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QNIVHSNGNTY (SEQ ID NO:56), KVS (SEQ ID NO:25), and LQGSNCSNH (SEQ ID NO:57) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GYEFTDFE (SEQ ID NO:50), FDPETGRS (SEQ ID NO:51), and SRFHYYGRTAY (SEQ ID NO:52),
wherein the 8C2.9 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLLNSRARKNY (SEQ ID NO:40), WAS (SEQ ID NO:34), and KQSYNLWT (SEQ ID NO:35) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFTFSNYY (SEQ ID NO:53), IKSNGVST (SEQ ID NO:54), and VRHDGYYFAY (SEQ ID NO:55), and
wherein the 4F1.7 monoclonal antibody comprises a light chain CDR1, CDR2, and CDR3 domain with the respective sequences of QSLFNSRARKNY (SEQ ID NO:49), WAS (SEQ ID NO:34), and KQSYNLWT (SEQ ID NO:35) and comprises a heavy chain CDR1, CDR2, and CDR3 domain with the respective sequences of GFSIKDTT (SEQ ID NO:58), IDPTDGHN (SEQ ID NO:59), and KQSYNLWT (SEQ ID NO:60).
8. The method of claim 7 wherein the purified chimeric antibody comprises the sequence of the six CDR domains of the 7H4.25 monoclonal antibody.
9. The method of claim 7 wherein the purified chimeric antibody is humanized.
10. The method of claim 7 wherein the purified chimeric antibody is recombinant.
11. The method of claim 10 , wherein the recombinant chimeric antibody comprises the sequence of the six CDR domains from the 7H4.25 monoclonal antibody.
12. The method of claim 7 , wherein the purified chimeric antibody is a single chain antibody.
13. The method of claim 7 , further comprising administering an antibiotic or a Staphylococcal vaccine composition.