Anti-presepsin antibody
The present invention provides methods and compositions for determining sepsis in an individual. Specifically, the present invention provides for antibodies of fragments thereof that specifically bind to presepsin. The antibodies of the present invention may be monoclonal antibodies, and they may specifically bind to a particular epitope of presepsin. The present invention further provides methods of using such antibodies to determine whether an individual has sepsis, and kits comprising the disclosed antibodies.
1. An anti-presepsin monoclonal antibody or an antigen-binding antibody fragment thereof, comprising a variable heavy (VH) domain with three complementarity determining regions (CDRs) and a variable light (VL) domain comprising three CDRs, the VH and VL domains comprising:
a. a first VH domain comprising
i. VH CDR1 consisting of an amino acid sequence of SEQ ID NO.: 7,
ii. VH CDR2 consisting of an amino acid sequence of SEQ ID NO.: 8, and
iii. VH CDR3 consisting of an amino acid sequence of SEQ ID NO.: 9, and
b. a first VL domain comprising
i. VL CDR1 consisting of an amino acid sequence of SEQ ID NO.: 22,
ii. VL CDR2 consisting of an amino acid sequence of SEQ ID NO.: 23, and
iii. VL CDR3 consisting of an amino acid sequence of SEQ ID NO.: 24; or
c. a second VH domain comprising
i. VH CDR1 consisting of an amino acid sequence of SEQ ID NO.: 7,
ii. VH CDR2 consisting of an amino acid sequence of SEQ ID NO.: 97, and
iii. VH CDR3 consisting of an amino acid sequence of SEQ ID NO.: 9, and
d. a second VL domain comprising
i. VL CDR1 consisting of an amino acid sequence of SEQ ID NO.: 22,
ii. VL CDR2 consisting of an amino acid sequence of SEQ ID NO.: 23, and
iii. VL CDR3 consisting of an amino acid sequence of SEQ ID NO.: 24; or
e. a third VH domain comprising
i. VH CDR1 consisting of an amino acid sequence of SEQ ID NO.: 7,
ii. VH CDR2 consisting of an amino acid sequence of SEQ ID NO.: 8, and
iii. VH CDR3 consisting of an amino acid sequence of SEQ ID NO.: 94, and
f. a third VL domain comprising
i. VL CDR1 consisting of an amino acid sequence of SEQ ID NO.: 22,
ii. VL CDR2 consisting of an amino acid sequence of SEQ ID NO.: 23, and
iii. VL CDR3 consisting of an amino acid sequence of SEQ ID NO.: 24;
wherein the antibody or the fragment specifically recognizes a peptide consisting of an amino acid sequence of SEQ ID NO.: 1.
2. The antibody or the antigen-binding antibody fragment thereof according to claim 1 , wherein the binding between the antibody or the fragment and presepsin is competitively-inhibited by 50% or more in a reaction system wherein a peptide consisting of a sequence of SEQ ID NO.: 1 is subjected to competitive reaction (absorbance) so that the binding between the antibody or the fragment and presepsin is inhibited.
3. The antibody or the antigen-binding antibody fragment according to claim 1 , wherein the competitive inhibition for the binding between the antibody or the fragment and presepsin by a peptide is less than 20%, wherein the peptide consists of a variant of Sequence ID No.1 in which the aspartic acid at position 8 is substituted with alanine.
4. The antibody or the antigen-binding antibody fragment thereof according to claim 1 , wherein the antibody or the fragment binds to presepsin in less than 10 −8 M of an affinity (KD).
5. The antibody or the antigen-binding antibody fragment thereof according to claim 1 , wherein the antibody or the fragment is produced using a peptide according to SEQ ID NO.: 2 as an administration antigen.
6. The antibody or the antigen-binding antibody fragment thereof according to claim 1 , wherein the antibody or the fragment does not specifically bind to high molecular weight soluble CD14.
7. The antibody or the antigen-binding antibody fragment thereof according to claim 1 , wherein the ratio of the sample which exhibits the separation degree of the presepsin measurement value of ±20% or less at the time of having TG concentration of 20 mg/mL in a sample indicates 50% or more in TG interference test on multiple samples performed by using the above antibody or the fragment.
8. An anti-presepsin monoclonal antibody or an antigen-binding antibody fragment thereof comprising,
a. a first VH domain comprising
i. VH CDR1 consisting of an amino acid sequence of SEQ ID NO.: 7,
ii. VH CDR2 consisting of an amino acid sequence of SEQ ID NO.: 8, and
iii. VH CDR3 consisting of an amino acid sequence of SEQ ID NO.: 9, and
b. a first VL domain comprising
i. VL CDR1 consisting of an amino acid sequence of SEQ ID NO.: 22,
ii. VL CDR2 consisting of an amino acid sequence of SEQ ID NO.: 23, and
iii. VL CDR3 consisting of an amino acid sequence of SEQ ID NO.: 24; or
c. a second VH domain comprising
i. VH CDR1 consisting of an amino acid sequence of SEQ ID NO.: 7,
ii. VH CDR2 consisting of an amino acid sequence of SEQ ID NO.: 97, and
iii. VH CDR3 consisting of an amino acid sequence of SEQ ID NO.: 9, and
d. a second VL domain comprising
i. VL CDR1 consisting of an amino acid sequence of SEQ ID NO.: 22,
ii. VL CDR2 consisting of an amino acid sequence of SEQ ID NO.: 23, and
iii. VL CDR3 consisting of an amino acid sequence of SEQ ID NO.: 24; or
e. a third VH domain comprising
i. VH CDR1 consisting of an amino acid sequence of SEQ ID NO.: 7,
ii. VH CDR2 consisting of an amino acid sequence of SEQ ID NO.: 8, and
iii. VH CDR3 consisting of an amino acid sequence of SEQ ID NO.: 94, and
f. a third VL domain comprising
i. VL CDR1 consisting of an amino acid sequence of SEQ ID NO.: 22,
ii. VL CDR2 consisting of an amino acid sequence of SEQ ID NO.: 23, and
iii. VL CDR3 consisting of an amino acid sequence of SEQ ID NO.: 24.
9. The antigen-binding antibody fragment according to claim 1 , wherein the fragment is an antigen-binding antibody fragment selected from the group consisting of Fab, Fab′, F (ab′)2, single-stranded antibody (scFv), dimerized V region (diabody), disulfide-stabilized V region (dsFv), sc (Fv)2, and a polypeptide comprising a heavy chain variable region and a polypeptide comprising a light chain variable region.
10. A polynucleotide that encodes the antibody or the antigen-binding antibody fragment thereof according to claim 1 .
11. A recombinant vector comprising the polynucleotide according to claim 10 .
12. A transformed strain obtained by introducing the recombinant vector according to claim 11 to a host cell.
13. The transformed strain according to claim 12 , wherein the host cell is a CHO cell.
14. A method of producing an antibody or an antigen-binding antibody fragment thereof, wherein the method comprises the step of culturing the transformed strain according to claim 12 .
15. A kit for measuring presepsin, wherein the kit comprises at least the antibody or the antigen-binding antibody fragment according to claim 1 .
16. The kit according to claim 15 , wherein the kit is a kit for detecting sepsis or assisting detection/diagnosis of sepsis.