Diagnostic method employing HNL
The present invention relates to the means and methods for the detection of bacterial infections, methods discriminating between viral and bacterial infections, methods of stratifying patients for subsequent treatment and further diagnostic purposes and methods to monitor antibiotherapy. The present invention is based on the detection of specific epitopes of human neutrophil lipocalin (HNL) using specific binding agents.
1. A binding agent configured to specifically bind to a polypeptide epitope of human neutrophil lipocalin (HNL) with a binding affinity,
wherein the binding agent comprises six murine complementarity-determining regions (CDRs),
wherein each of the CDRs are configured to bind to amino acids 141 to 156 of the human polypeptide epitope of HNL as defined in SEQ ID NO: 1,
wherein the HNL epitope is specifically bound,
wherein the binding affinity is at least 75% or higher compared with a binding specificity achieved with the CDRs, wherein the CDRs are depicted in SEQ ID Nos: 8 to 13, 14 to 19, or 20 to 25,
wherein the binding agent comprises a heavy chain variable region and a light chain variable region,
wherein the heavy chain variable region comprises a first set of the murine CDRs, the first set comprising:
a first heavy chain CDR (CDRH1), wherein CDRH1 is SEQ ID NO: 11;
a second heavy chain CDR (CDRH2), wherein CDRH2 is SEQ ID NO: 12; and
a third heavy chain CDR (CDRH3), wherein CDRH3 is SEQ ID NO: 13,
wherein the light chain variable region comprises a second set of the murine CDRs, the second set comprising:
a first light chain CDR (CDRL1), wherein CDRL1 SEQ ID NO: 8;
a second light chain CDR (CDRL2), wherein CDRL2 SEQ ID NO: 9; and
a third light chain CDR (CDRL3), wherein CDRL3 SEQ ID NO: 10.
2. The binding agent according to claim 1 ,
wherein the binding agent has a heavy chain comprising the first set,
wherein the heavy chain comprises a heavy chain variable region sequence selected from the group consisting of sequences depicted in SEQ ID NO: 3,
wherein the binding agent has a light chain comprising the second set,
wherein the light chain comprises a light chain variable region sequence selected from the group consisting of sequences depicted in SEQ ID NO: 2.
3. A diagnostic composition comprising a binding agent as defined in claim 1 .
4. A diagnostic kit comprising containers comprising a binding agent as defined in in claim 1 , and at least one of instructions for use, buffers, and a device, wherein the device is arranged for blood, plasma, serum, urine, cerebrospinal fluid (CSF), bone marrow, saliva, or sputum sample analysis.
5. The binding agent according to claim 1 , wherein the binding agent is a monoclonal antibody, a chimeric antibody, or a humanized antibody.
6. The binding agent according to claim 1 ,
wherein the binding agent has a heavy chain comprising the first set of,
wherein the heavy chain comprises a sequence depicted in SEQ ID NO: 3.
7. The binding agent according to claim 1 ,
wherein the binding agent has a light chain comprising the second set,
wherein the light chain comprises a sequence depicted in SEQ ID NO: 2.