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Human Monoclonal Antibodies Against CD20

a technology of monoclonal antibodies and cd20, which is applied in the field of human monoclonal antibodies against cd20, can solve the problems that current available murine and chimeric antibodies do not constitute ideal therapeutic agents, and achieve the effect of less immunogenicity

Inactive Publication Date: 2014-04-03
GENMAB AS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

The patent describes a new feature or improvement that is related to a certain technology or invention. The purpose of the patent is to explain the new feature or improvement in detail, so that people can understand it better. In simple terms, the patent is trying to explain a special tool or process that helps achieve a certain technical effect.

Problems solved by technology

However, while the results obtained to date clearly establish CD20 as a useful target for immunotherapy, they also show that currently available murine and chimeric antibodies do not constitute ideal therapeutic agents.

Method used

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  • Human Monoclonal Antibodies Against CD20
  • Human Monoclonal Antibodies Against CD20
  • Human Monoclonal Antibodies Against CD20

Examples

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Effect test

example 1

Production of Human Antibodies Against CD20

[0367]HCo7 and KM Mice:

[0368]Fully human monoclonal antibodies to CD20 were prepared using HCo7 and KM mice which express human antibody genes. In the KM mouse strain, the endogenous mouse kappa light chain gene has been homozygously disrupted as described in Chen et al. (1993) EMBO J. 12:811-820 and the endogenous mouse heavy chain gene has been homozygously disrupted as described in Example 1 of PCT Publication WO 01 / 09187. This mouse strain carries a human kappa light chain transgene, KCo5, as described in Fishwild et al. (1996) Nature Biotechnology 14:845-851. This mouse strain also carries a human heavy chain transchromosome composed of chromosome 14 fragment hCF (SC20) as described in WO 02 / 43478.

[0369]The HCo7 mice have a JKD disruption in their endogenous light chain (kappa) genes (as described in Chen et al. (1993) EMBO J. 12: 821-830), a CMD disruption in their endogenous heavy chain genes (as described in Example 1 of WO 01 / 14424...

example 2

Antibody Sequencing of Human Antibodies Against CD20

Sequencing of the VL and VH Regions

[0384]RNA Preparation:

[0385]Total RNA was prepared from 5×106 cells of all HuMAb CD20 hybridoma cell lines (2F2, 7D8 and 11B8) with RNeasy kit (Qiagen, Westburg, Leusden, Netherlands) according to the manufacturer's protocol.

[0386]cDNA Preparation of 2F2 and 7D8:

[0387]5′-RACE-Ready Complementary DNA (cDNA) of RNA was prepared from 1 μg total RNA, using the SMART RACE cDNA Amplification kit (Clonetech), following the manufacturer's protocol.

VH and VL regions were amplified using an advantage HF 2 PCR Kit (Clonetech, BD) and using the following primers:

VK RACE25′ GCA GGC ACA CAA CAG AGG CAG TTC CAG ATT TCanneals in C-kappaVH RACE25′ GCT GTG CCC CCA GAG GTG CTC TTG GAG Ganneals in CHl

[0388]cDNA Preparation of 11B8:

[0389]Complementary DNA (cDNA) of RNA from 11B8 cells was prepared from 3 μg total RNA with AMV Reverse Transcriptase with buffer (Roche Diagnostics GmbH, Mannheim, Germany), oligo d(T)15 (...

example 3

Recombinant Production of 2F2 and 11B8 in GS-NS / 0 Cell Line

[0403]2F2T:

[0404]The heavy chain and light chain variable regions of the 2F2 antibody were amplified, using PCR, from a standard cloning vector, pGem-5Zf (Promega), using primers which included an optimal Kozak sequence and suitable restriction sites to clone the fragments in the GS constant region vectors pCONγ1f and PCONκ (Lonza).

[0405]After amplification, the fragments were purified and digested with the restriction enzymes for cloning and ligated in the two vectors. The heavy chain variable fragment was digested with Hind III and Bsi WI and ligated into the pCONγ1f vector which had been digested with Hind III and Bsi WI, and dephosphorylated with alkaline phosphatase. The light chain variable fragment was digested with Hind III and Apa I and ligated into the PCONκ vector which had been digested with Hind III and Apa I, and dephosphorylated with alkaline phosphatase. The pCONγ1f / variable-heavy and PCONκ / variable-light vec...

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Abstract

Isolated human monoclonal antibodies which bind to and inhibit human CD20, and related antibody-based compositions and molecules, are disclosed. The human antibodies can be produced by a transfectoma or in a non-human transgenic animal, e.g., a transgenic mouse, capable of producing multiple isotypes of human monoclonal antibodies by undergoing V-D-J recombination and isotype switching. Also disclosed are pharmaceutical compositions comprising the human antibodies, non-human transgenic animals and hybridomas which produce the human antibodies, and therapeutic and diagnostic methods for using the human antibodies.

Description

RELATED APPLICATIONS[0001]This application claims priority to U.S. Provisional Application No. 60 / 419,163, filed on Oct. 17, 2002, and U.S. Provisional Application No. 60 / 460,028, filed on Apr. 2, 2003, both entitled HUMAN MONOCLONAL ANTIBODIES AGAINST CD20, and both of which are incorporated herein in their entirety by this reference.BACKGROUND OF THE INVENTION[0002]The CD20 molecule (also called human B-lymphocyte-restricted differentiation antigen or Bp35) is a hydrophobic transmembrane protein with a molecular weight of approximately 35 kD located on pre-B and mature B lymphocytes (Valentine et al. (1989)J. Biol. Chem. 264(19):11282-11287; and Einfield et al. (1988) EMBO J. 7(3):711-717). CD20 is found on the surface of greater than 90% of B cells from peripheral blood or lymphoid organs and is expressed during early pre-B cell development and remains until plasma cell differentiation. CD20 is present on both normal B cells as well as malignant B cells. In particular, CD20 is ex...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07K16/28A61K45/06G01N33/68A61K39/395A61K39/00C07K16/42C12N5/22C12N5/24
CPCC07K16/2887G01N33/686A61K45/06A61K39/3955A61K2039/505C07K16/4258C07K2317/21C07K2317/54C07K2317/56C07K2317/72C07K2317/732C07K2317/734C07K2317/92A61P1/00A61P1/04A61P11/00A61P11/06A61P13/12A61P17/00A61P17/06A61P17/08A61P19/02A61P21/04A61P25/00A61P25/28A61P27/02A61P29/00A61P31/18A61P31/20A61P31/22A61P35/00A61P35/02A61P37/00A61P37/02A61P37/06A61P37/08A61P43/00A61P5/14A61P7/00A61P7/04A61P7/06A61P9/08A61P9/10A61P9/14A61P3/10C07K16/28C07K16/30C12N5/16
Inventor TEELING, JESSICARUULS, SIGRIDGLENNIE, MARTINVAN DE WINKEL, JAN G.J.PARREN, PAULPETERSEN, JORGENBAADSGAARD, OLEHUANG, HAICHUN
Owner GENMAB AS
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