Animal Models and Therapeutic Molecules

Abstract

The invention discloses methods for the generation of chimaeric human-non-human antibodies and chimaeric antibody chains, antibodies and antibody chains so produced, and derivatives thereof including fully humanised antibodies; compositions comprising said antibodies, antibody chains and derivatives, as well as cells, non-human mammals and vectors, suitable for use in said methods.

1 . A method for producing a biological sample selected from the group consisting of:
 (i) a polypeptide comprising a human kappa variable region,   (ii) an Ig kappa light chain comprising a human kappa variable region,   (iii) an antibody comprising a human kappa variable region,   (iv) a cell expressing a polypeptide comprising a human kappa variable region,   (v) a cell expressing an Ig kappa light chain comprising a human kappa variable region,   (vi) a cell expressing an antibody comprising a human kappa variable region,   (vii) nucleic acid encoding a polypeptide comprising a human kappa variable region,   (viii) variable region, and   (ix) nucleic acid encoding a human kappa variable region,   
       the method comprising the step of isolating said biological sample from a mouse or a cell encoding said human kappa variable region, 
       wherein said human kappa variable region is of a transgenic mouse having been stimulated with an antigen and having a germline comprising a homozygous recombinant immunoglobulin light chain kappa (Igκ) locus comprising unrearranged human Igκ variable region gene segments at an endogenous mouse kappa light chain locus upstream of a kappa enhancer and a constant (C) region comprising an endogenous Ck gene segment wherein said recombinant Igκ locus comprises in 5′ to 3′transcriptional orientation unrearranged human Igκ variable region gene segments, a chimeric JC intron comprising truncated human Igκ JC intronic DNA, truncated mouse Igκ JC intronic DNA comprising said kappa enhancer, and said constant (C) region wherein said human Igκ variable region gene segments in said recombinant Igκ locus are operably linked in said C region, and wherein said unrearranged Igκ variable region gene segments comprise human Vκ4-1, Vκ5-2, Vκ7-3, Vκ2-4, Vκ1-5, Vκ1-6, Vκ3-7, Vκ1-8, Vκ1-9, Jκ1, Jκ2, Jκ3, Jκ4, and Jκ5 gene segments; 
       wherein the germline of said transgenic mouse is homozygous for a chimeric IgH locus comprising unrearranged human IgH variable region gene segments, at an endogenous IgH locus upstream of an enhancer and a constant (C) region comprising an endogenous CH gene segment, wherein said unrearranged human variable region gene segments comprise unrearranged human VH region gene segments comprising a plurality of human VH, JH, and D gene segments in said chimeric IgH locus are operably linked to said enhancer and said C region; wherein said germline comprises all or part of mouse IgH variable region DNA upstream of said unrearranged human VH region gene segments comprising the human VH, D and JH gene segments; wherein said transgenic mouse is non-functional to express fully mouse Ig comprising a mouse VH region and a mouse CH region; 
       wherein said transgenic mouse prior to said antigen stimulation comprises B cells comprising said recombinant Igκ locus, and wherein after said antigen stimulation, said transgenic mouse comprises B cells comprising antibody specific for said antigen and comprising light chain comprising a human kappa variable region; 
       wherein said IgH locus of said transgenic mouse is capable of undergoing V, D, J joining and wherein said transgenic mouse, following said stimulation with said antigen, is capable of producing a plurality of antibodies specific for said antigen comprising a chimeric Ig heavy chain comprising a plurality of human IgH chain variable regions; 
       wherein said recombinant immunoglobulin light chain kappa (Igκ) locus of said transgenic mouse is capable of undergoing V, J joining; 
       wherein said transgenic mouse, following stimulation with said antigen, is capable of producing a plurality of antibodies specific for said antigen comprising a chimeric Igκ chain comprising a plurality of human Igκ chain variable regions; and 
       wherein said transgenic mouse is capable of breeding with another said transgenic mouse to provide subsequent generation mice, wherein said subsequent generation mouse comprises: (i) in its germline said homozygous IgH locus, (ii) in its germline comprising all or part of mouse IgH variable region DNA upstream of said unrearranged human VH region gene segments, and capable of breeding to subsequent generations, and wherein said subsequent generation mouse is capable of breeding with a said subsequent generation mouse to further subsequent generations. 
     
     
         2 . The method of  claim 1 , further comprising the step of providing a fully human Igκ polypeptide by recombinantly replacing said mouse constant region comprising an endogenous Ck gene segment with a human kappa constant region. 
     
     
         3 . The method of  claim 1 , wherein said isolated biological sample comprises a cell which is a B cell comprising said antigen-specific antibody, and said method further comprises the step of preparing a hybridoma from said B cell. 
     
     
         4 . The method of  claim 3 , wherein said method further comprises the step of isolating nuclei acid from said hybridoma, wherein said nucleic acid encodes a polypeptide selected from the group consisting of: said human kappa variable region, a light chain polypeptide comprising said human kappa variable region, or said antigen-specific antibody comprising said human kappa variable region. 
     
     
         5 . The method of  claim 4 , further comprising combining nucleic acid encoding a human kappa variable region with nucleic acid encoding a human kappa constant region, thereby producing a nucleic acid encoding a human Igκ polypeptide. 
     
     
         6 . The method of  claim 5 , further comprising inserting said nucleic acid encoding said fully human Igκ peptide into the genome of a cell, thereby providing a cell capable of expressing said human Igκ polypeptide. 
     
     
         7 . The method of  claim 6 , further comprising the step of:
 expressing said human Igκ polypeptide from said cell, and optionally isolating the expressed polypeptide.   
     
     
         8 . The method of  claim 7 , further comprising the step of:
 expressing in vitro said human Igκ polypeptide from said nucleic acid encoding said human Igκ polypeptide, and optionally isolating the expressed polypeptide.   
     
     
         9 . The method of  claim 1 , wherein said antigen is a human antigen. 
     
     
         10 . The method of  claim 1 , wherein said isolated biological sample comprises a cell which is a B cell comprising said human kappa variable region, or a B cell expressing said antigen-specific antibody, and said method further comprises the step of isolating nucleic acid from a B-cell, wherein said nucleic acid encodes said human kappa variable region, or said antigen-specific antibody comprising said Igκ polypeptide. 
     
     
         11 . The method of  claim 10 , further comprising combining nucleic acid encoding said human kappa region with nucleic acid encoding a human constant region, thereby producing a nucleic acid encoding a human Igκ polypeptide. 
     
     
         12 . The method of  claim 11 , further comprising the step of: expressing in vitro or in vivo from a cell said human Igκ polypeptide from said nucleic acid encoding a fully human polypeptide comprising said huma kappa variable region and a human C region, and optionally isolating the expressed polypeptide. 
     
     
         13 . The method of  claim 1 , wherein said isolated biological sample comprises nucleic acid encoding said human kappa variable region, and said method further comprises the step of: combining said nucleic acid encoding said human kappa variable region to nucleic acid encoding a human C region polypeptide to produce nucleic acid encoding a fully human polypeptide comprising said human kappa variable region and said human C region. 
     
     
         14 . The method of  claim 13 , further comprising the step of: expressing in vitro or in vivo from a cell said fully human polypeptide from said nucleic acid encoding a fully human polypeptide comprising said human kappa variable region and a human a human C region. 
     
     
         15 . The method of  claim 12 , further comprising isolating said fully human polypeptide and combining said polypeptide with a human heavy chain polypeptide to provide an antibody. 
     
     
         16 . The method of  claim 1 , wherein said kappa enhancer is a mouse kappa enhancer. 
     
     
         17 . The method of  claim 16 , wherein said human JK gene segments comprise a 3′ human Jκ gene segment and wherein the distance from said 3′ human Jκ gene segment to said mouse IgK JC intronic DNA is less than 2 kb. 
     
     
         18 . The method of  claim 16 , wherein the distance between said mouse IgK JC intronic DNA and said mouse enhancer comprises 782 bp. 
     
     
         19 . The method of  claim 16 , wherein DNA between said mouse IgK JC intronic DNA and said enhancer comprises mouse 129 strain JC intronic DNA. 
     
     
         20 . The method of  claim 1 , wherein 100% of B-cells of said mouse after antigen stimulation comprise Vκ and Jκ gene segments.