Antibodies to human erythroferrone and uses thereof
AssigneeIntrinsic Lifesciences LLC
InventorsMark Westerman, Huiling Han, Vaughn Ostland
Life of this patent
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Abstract
Disclosed herein are antibodies specific for erythroferrone and assays comprising the antibodies. Also disclosed are methods for using the assays for the diagnosis or monitoring of disease.
Claims20
A method of assessing erythropoiesis in a subject with a disorder associated with erythroferrone (ERFE) or myonectin, comprising subjecting a sample from the subject to an assay comprising:
- contacting the sample with a first antibody to form a first antibody-ERFE complex;
- and then detecting the presence of and/or measuring the amount of a second antibody bound to the first antibody-ERFE complex, wherein the first antibody and the second antibody are not the same and each are independently an ERFE-binding antibody, or an ERFE-binding fragment thereof, the antibodies selected from:
- (a) an antibody comprising a heavy chain variable region (VH) and a light chain variable region (VL), wherein
- (i) the VH comprises the amino acid sequence of SEQ ID NO:18 and the VL comprises the amino acid sequence of SEQ ID NO:23;
- (ii) the VH comprises the amino acid sequence of SEQ ID NO:28 and the VL comprises the amino acid sequence of SEQ ID NO:33;
- (iii) the VH comprises the amino acid sequence of SEQ ID NO:38 and the VL comprises the amino acid sequence of SEQ ID NO:43;
- (iv) the VH comprises the amino acid sequence of SEQ ID NO:48 and the VL comprises the amino acid sequence of SEQ ID NO:53;
- or
- (v) the VH comprises the amino acid sequence of SEQ ID N0:58 and the VL comprises the amino acid sequence of SEQ ID NO:63,
- or
- (b) an antibody comprising:
- (i) heavy chain complementarity determining regions (CDRs) having the amino acid sequences of SEQ ID NOs:19-21 and light chain CDRs having the amino acid sequences of SEQ ID NOs:24-26;
- (ii) heavy chain CDRs having the amino acid sequences of SEQ ID NOs:29-31 and light chain CDRs having the amino acid sequences of SEQ ID NOs:34-36;
- (iii) heavy chain CDRs having the amino acid sequences of SEQ ID NOs:39-41 and light chain CDRs having the amino acid sequences of SEQ ID NOs:44-46;
- (iv) heavy chain CDRs having the amino acid sequences of SEQ ID NOs:49-51 and light chain CDRs having the amino acid sequences of SEQ ID NOs:54-56;
- or
- (v) heavy chain CDRs having the amino acid sequences of SEQ ID NOs:59-61 and light chain CDRs having the amino acid sequences of SEQ ID NOs:64-66;
- thus determining the presence, and or the amount, of an ERFE protein in the sample.
A method of assessing erythropoiesis in a subject with a disorder associated with ERFE or myonectin, comprising contacting a sample from a subject with at least one ERFE-binding antibody, or ERFE-binding fragment thereof such that ERFE in the sample is detected and the antibody is selected from:
- (a) an antibody comprising a heavy chain variable region (VH) and a light chain variable region (VL), wherein
- (i) the VH comprises the amino acid sequence of SEQ ID NO:18 and the VL comprises the amino acid sequence of SEQ ID NO:23;
- (ii) the VH comprises the amino acid sequence of SEQ ID NO:28 and the VL comprises the amino acid sequence of SEQ ID NO:33;
- (iii) the VH comprises the amino acid sequence of SEQ ID NO:38 and the VL comprises the amino acid sequence of SEQ ID NO:43;
- (iv) the VH comprises the amino acid sequence of SEQ ID NO:48 and the VL comprises the amino acid sequence of SEQ ID NO:53;
- or
- (v) the VH comprises the amino acid sequence of SEQ ID N0:58 and the VL comprises the amino acid sequence of SEQ ID NO:63,
- or
- (b) an antibody comprising:
- (i) heavy chain complementarity determining regions (CDRs) having the amino acid sequences of SEQ ID NOs:19-21 and light chain CDRs having the amino acid sequences of SEQ ID NOs:24-26;
- (ii) heavy chain CDRs having the amino acid sequences of SEQ ID NOs:29-31 and light chain CDRs having the amino acid sequences of SEQ ID NOs:34-36;
- (iii) heavy chain CDRs having the amino acid sequences of SEQ ID NOs:39-41 and light chain CDRs having the amino acid sequences of SEQ ID NOs:44-46;
- (iv) heavy chain CDRs having the amino acid sequences of SEQ ID NOs:49-51 and light chain CDRs having the amino acid sequences of SEQ ID NOs:54-56;
- or
- (v) heavy chain CDRs having the amino acid sequences of SEQ ID NOs:59-61 and light chain CDRs having the amino acid sequences of SEQ ID NOs:64-66.
Dependencies are inferred from the claim text.