Wiki source code of Monoclonal antibodies production introduction
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1 | Monoclonal antibodies are antibodies which | ||
2 | have a single, selected specificity and which | ||
3 | are continuously secreted by ìimmortalisedî | ||
4 | hybridoma cells. A hybridoma is a biologi- | ||
5 | cally constructed hybrid of a mortal, anti- | ||
6 | body-producing, lymphoid cell, and a | ||
7 | malignant, or ìimmortalî, myeloma cell. Fol- | ||
8 | lowing the discovery of hybridoma technol- | ||
9 | ogy in 1975 , developments in mAb | ||
10 | production and in their application have had | ||
11 | profound implications not only on medical | ||
12 | research, diagnosis and therapy, but also on | ||
13 | biology in general. Hybridoma technology | ||
14 | represents a significant advance because, in | ||
15 | principle, it provides a means for obtaining | ||
16 | unlimited supplies of highly specific antibod- | ||
17 | ies. | ||
18 | In the production of mAbs, animals (gen- | ||
19 | erally rats or mice) first have to be immu- | ||
20 | nised with the target antigen to obtain | ||
21 | mortal antibody-producing cells. The biolog- | ||
22 | ical construction of hybrids, and the selec- | ||
23 | tion of hybridomas which produce antibodies | ||
24 | with the desired specificities, are carried out | ||
25 | in vitro | ||
26 | . In the early days of hybridoma tech- | ||
27 | nology (the late 1970s), the hybridomas | ||
28 | developed | ||
29 | in vitro | ||
30 | were injected into the peri- | ||
31 | toneal cavity of an animal so that useful | ||
32 | amounts of the desired mAb could be har- | ||
33 | vested from the ascitic fluid. This procedure | ||
34 | was considered necessary at the time, since | ||
35 | no efficient large-scale | ||
36 | in vitro | ||
37 | methods were | ||
38 | available. By the mid-1980s, there were | ||
39 | already serious doubts regarding the neces- | ||
40 | sity of such a painful animal procedure. Nev- | ||
41 | ertheless, as a result of its early introduction | ||
42 | as part of the hybridoma technology, ascites | ||
43 | production of mAbs is now employed world- | ||
44 | wide, in spite of the ongoing development | ||
45 | of | ||
46 | in vitro | ||
47 | technologies and the growing pub- | ||
48 | lic pressure to replace or reduce animal | ||
49 | experiments. The urgent need for experts to | ||
50 | disseminate information and make recom- | ||
51 | mendations about antibody production, tak- | ||
52 | ing animal welfare issues into consideration, | ||
53 | was recognised by ECVAM in holding a | ||
54 | workshop on avian antibodies in March 1996 | ||
55 | and, subsequently, in organising this | ||
56 | workshop on mAb production. | ||
57 | |||
58 | |||
59 | |||
60 | Related Tags : [[monoclonal antibody production]]http://www.ab-mart.com/index.html , [[monoclonal antibodies production]]http://www.ab-mart.com/index.html |