亚洲知识产权资讯网为知识产权业界提供一个一站式网上交易平台,协助业界发掘知识产权贸易商机,并与环球知识产权业界建立联系。无论你是知识产权拥有者正在出售您的知识产权,或是制造商需要购买技术以提高操作效能,又或是知识产权配套服务供应商,你将会从本网站发掘到有用的知识产权贸易资讯。

Production of Secretory IgA with Increased Stability

技术优势
Established IgA producing cell lines can be transfected with the SC component to produce sIgA with identical specificity. Can create new sIgA monoclonal antibodies produced in large quantities from a single cell line using standard antibody production techniques. sIgA has increased stability compared to currently available IgA monoclonal antibodies.
技术应用
Production of stable, sIgA monoclonal antibodies.
详细技术说明
UCLA researchers have developed a process to produce stable sIgA from a single mammalian cell in quantities practical for therapeutic uses. Vectors and cell lines for producing non-secretory IgA are readily available. In order to easily produce sIgA from these same cell types, a vector encoding the secretory signal is transfected into the IgA producing cell lines and stable transductants are cloned. In vitro and in vivo stability of the sIgA was measured and sIgA was found to have significantly greater stability than monoclonal IgA lacking SC. This invention provides a solution for the need for large quantities of sIgA monoclonal therapeutic antibodies.
*Abstract
None
*IP Issue Date
Oct 9, 2001
*Principal Investigation

Name: Koteswara Chintalacharuvu

Department:


Name: Sherie Morrison

Department:

附加资料
Patent Number: US6300104B1
Application Number: US199895385A
Inventor: Morrison, Sherie L. | Chintalacharuvu, Kote R.
Priority Date: 19 Jun 1997
Priority Number: US6300104B1
Application Date: 10 Jun 1998
Publication Date: 9 Oct 2001
IPC Current: A61K0039395 | A61P003704 | C07K001600 | C12P002104 | A61K003800
US Class: 43507021 | 4241331 | 4241411 | 4241471 | 4350701 | 4350702 | 4353201 | 435326 | 435328 | 435339 | 5303871 | 530808
Assignee Applicant: The Regents of the University of California
Title: Secretory immunoglobulin produced by single cells and methods for making and using same
Usefulness: Secretory immunoglobulin produced by single cells and methods for making and using same
Summary: USE The method is useful to produce commercial quantities of sIg (especially sIgA) to treat or prevent infections. In particular, sIgA produced by the method can be combined with a carrier in pharmaceutical compositions (claimed), which can be administered to prevent/treat infections (claimed) especially in mammals (particularly humans), birds or fish (claimed). Such compositions can be used to prevent or treat bacterial, viral, mycoplasmal, mycobacterial, yeast or parasitic infections, especially systemic infections or infections at a mucosal surface (claimed). They are especially useful to prevent or treat human infection with human immunodeficiency virus (HIV), respiratory syncytial virus, flu virus or cold virus (claimed). SIgA is usually found in external secretions such as colostrum, saliva, tears etc. and is often the first line of defence against infectious agents in the body.
Novelty: Producing secretory immunoglobulin in single cells useful to produce commercial quantities of secretory immunoglobulin to prevent or treat infections
主要类别
诊断/治疗
细分类别
人类免疫缺陷病毒
申请号码
6300104
其他

Background

The immunoglobulin secretory IgA (sIgA) is found in mucosal surfaces is often the first line of defense against infectious agents. Normally, sIgA is the product of two different cell types with heavy, light, and J chains produced by plasma cells, whereas the secretory component (SC) is added by cellular enzymes during transit of the dimeric IgA through the epithelial cell layer.The SC component of sIgA provides for stability at the mucosal surfaces. Currently available monoclonal IgA which lacks SC, while protective, is rapidly degraded. Attempts have been made to create sIgA in vitro by either co-culturing IgA producing cells with polarized epithelial cells or by adding SC exogenously to purified IgA, however, both methods provide very low yields of sIgA.


Additional Technologies by these Inventors


Tech ID/UC Case

20097/1997-545-0


Related Cases

1997-545-0

国家/地区
美国

欲了解更多信息,请点击 这里
移动设备