Talk:Nomenclature of monoclonal antibodies

Latest comment: 3 years ago by Mys 721tx in topic Editorializing
Good articleNomenclature of monoclonal antibodies has been listed as one of the Natural sciences good articles under the good article criteria. If you can improve it further, please do so. If it no longer meets these criteria, you can reassess it.
Article milestones
DateProcessResult
February 21, 2011Good article nomineeListed
Did You Know
A fact from this article appeared on Wikipedia's Main Page in the "Did you know?" column on July 12, 2006.
The text of the entry was: Did you know ...that there is a pattern to the names of the class of medications called "monoclonal antibodies"?

Table borders

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Could somebody fix the table, please? The borders are not correct. NCurse work 14:26, 9 July 2006 (UTC)Reply

Hmm. I tried several different things and wasn't able to fix it. I'll try asking at the Village Pump. — Knowledge Seeker 07:54, 10 July 2006 (UTC)Reply
OK, never mind, I used a quite inelegant solution. — Knowledge Seeker 08:19, 10 July 2006 (UTC)Reply

Merger of stems

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Merger of -mab stems: -amab, -emab, -imab, -omab, -umab, -ximab, -zumab, and -axomab was proposed by BlakeCS on 30 December 2006. I agree that this information could be placed in a single table in this, the Nomenclature of monoclonal antibodies article. --Bejnar 19:21, 30 December 2006 (UTC)Reply

No, I think redirection is in order at this point. — Swpb talk contribs 06:19, 31 December 2006 (UTC)Reply
Done. — Swpb talk contribs 08:08, 1 January 2007 (UTC)Reply

New stems

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Stems what I've made up is: murine hybrids: -exomab, -ixomab, -oxomab, and -uxomab. Two-letter combinations for targets: -o(s). Three-letter combinations for targets: -mu(l)- (muscular). Four-letter combinations for targets: -neu(r)- (nervous system), -tox(a)- (toxin), -fu(ng)- (fungal). -xomab means a murine hybrid. BlakeCS 05:45, 21 January 2007 (UTC)Reply

Examples

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I think this page might be more accessible to beginners if several more examples were given and analyzed. This nomenclature is unique, and it takes a while to get your mind around it.

A linguist might say that these words are agglutinative, with a string of components but no definite stem (if -mab is viewed as a stem, then words might be called synthetic). Whole languages can be agglutinative, like spoken French or like the Algonkian languages of North America, or synthetic like Latin, Sanskrit, or Turkish.

Either way, they don't work like English, and the learner needs all the help he can get.

Or maybe this elderly physician just needs to retire!

Bob Richmond (talk) 00:35, 1 November 2008 (UTC)Bob RichmondReply

To do

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--ἀνυπόδητος (talk) 16:27, 8 June 2010 (UTC)Reply

GA Review

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Reviewing
This review is transcluded from Talk:Nomenclature of monoclonal antibodies/GA1. The edit link for this section can be used to add comments to the review.

Will be adding comments later tonight. Reviewer: JFW | T@lk 20:29, 10 February 2011 (UTC)Reply

Initial comments

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  • Introduction:
    • The reader who doesn't know what monoclonal antibodies are should perhaps be introduced to the concept in 2-3 brief sentences. Difficult, but not impossible.
    • Do we need to delve into the fragments in the intro? It needs quite a lot of context to be understandable, and might be better in the body somewhere.
    • In the table, some items in the list are under discussion "as of February 2010". Have any conclusions been reached, or is this still the state of affairs?
  • Components:
    • Antibodies from hamsters (theoretically -e-) and primates (-i-) have never been assigned INNs. This might benefit from rephrasing, such as: "No INN has ever been requested for antibodies from hamsters [...]". Do any sources explain why they were anticipated, and why none were assigned?
      • Rephrased. I'm pretty sure I know the answers to your questions. Will look for sources. --ἀνυπόδητος (talk) 14:27, 12 February 2011 (UTC)Reply
      • Tough one. These animals are more or less closely related to humans (see Euarchontoglires), making immunogenicity less of a problem, and they are easy to keep as laboratory animals. But this doesn't explain why there is no substem for rabbits. Regarding your second question: Mice seem to be the most commonly used hosts, presumably for practical reasons (small, breed quickly, well known biological properties). It isn't impossible, though, that primate mabs will receive INNs in the future. However, that's all guesswork; I didn't find any good sources. Will ask at WT:PHARM. --ἀνυπόδητος (talk) 19:46, 14 February 2011 (UTC)Reply
    • It might help if the image were modified to show the CDRs more clearly, as not all readers will know what these are and why they matter.
       
    • With regards to the "prefix" section, it could be pointed out that different commercial antibodies for exactly the same target (don't know if this has happened) would have different prefixes to distinguish them. Unsure if the sources might help here.
    • With regards to "additional words", I think a few examples would be immensely helpful here.
      •   Done. The last two "Old convention" bullets are now somewhat redundant. Do you think I can remove them? (An example of the type isotope + mab [Technetium (99mTc) pintumomab] could be added to the "additional words" section"). --ἀνυπόδητος (talk) 17:32, 13 February 2011 (UTC)Reply
  • History:

An interesting article! Let me know how you get on with the above points. I expect there might be one or two other small things, on the whole it looks good. JFW | T@lk 23:40, 10 February 2011 (UTC)Reply

Done, more or less. I am still looking for a source saying that mabs were discovered in multiple myeloma (nothing found, removed sentence --ἀνυπόδητος (talk) 10:59, 19 February 2011 (UTC)), and have more or less given up on the question why there are no hamster mabs.Reply
Could you comment on my question whether to remove/merge the redundant examples? Thanks, ἀνυπόδητος (talk) 15:48, 18 February 2011 (UTC)Reply
I don't think we need to have a separate section with examples if we're already providing examples in context.
Will hopefully do a final review later tonight. JFW | T@lk 21:01, 19 February 2011 (UTC)Reply

Things definitely looking good. You have clearly followed up my recommendations. I think that despite the slight redundancy, the "examples" section still enhances the article, and should probably remain.

The use of the {{cite doi}} and {{cite pmid}} templates means that it is slightly more different to force all references into a consistent format (e.g. spaces vs semicolons between authors). I have no immediate solution for this, and it is one of the reasons why I personally generate my citations templates by other means. I don't think this is a breaking point for WP:WIAGA.

I will give the article a final read tomorrow and probably pass for GA at that point. JFW | T@lk 23:32, 19 February 2011 (UTC)Reply

Last few bits

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A quick final readthrough has identified the following two points:

  • I struggled to differentiate variable regions and CDRs. Would it be possible to expand on this very briefly?
  • If you are going to rely on {{cite doi}} and {{cite pmid}}, would it be possible to make all other references consistent? By this I mean using the same style for the names of the authors (comma after the surname, semicolon after the initials). I personally favour the Surname IN, Othersurname AB. format, but as long as things are consistent it's fine. Hate to harp on about this, but it technically falls under WP:WIAGA 1b.
    • I don't think the format has something to do with {{cite doi}} vs {{citation}} but rather with the use of parameters (authors= vs last1= | first1= etc). I prefer using the latter, resulting in Surname, IN; Othersurname, AB, because it's better machine readable and I can see no disadvantage for human readers. Hope that's fine with you.
      • That's fine. I think both the templates use the citation bot, which formats references differently from Diberri's template filler. As long as things are consistent, it's all good. JFW | T@lk 20:37, 21 February 2011 (UTC)Reply
    • Ref #18 only gives "AGN" as an author, and I'm not sure whether I've placed the "Jr." correctly in #4, but apart from that I think I've caught everything. --ἀνυπόδητος (talk) 11:04, 21 February 2011 (UTC)Reply

Otherwise passable without a question. JFW | T@lk 10:34, 21 February 2011 (UTC)Reply

  Passed GA assessment. Well done and particular commendations for your patience! JFW | T@lk 20:37, 21 February 2011 (UTC)Reply
Thanks for your review! I enjoyed your constructive suggestions, and the article is now definitely better and more complete than two weeks ago. --ἀνυπόδητος (talk) 21:16, 21 February 2011 (UTC)Reply

Misleading article title

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Could I just point out that this article is not about the nomenclature of monoclonal antibodies? It is about the nomenclature of *therapeutic* monoclonal antibodies. A monoclonal antibody can be called anything you like. It is only when a monoclonal antibody which is intended to become a drug reaches the stage of development where an INN is required that the system so tortuously described in the article kicks in.

Target substem

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The USAN 2019 Naming Policy states that "[t]he target infix places information about the action or use of the antibody in the name", which is in conflict with the currently unsourced text in the article. I have yet to find any information from WHO literature. I will remove those paragraph if there are no evidence otherwise. -Mys_721tx (talk) 18:28, 6 December 2020 (UTC)Reply

Editorializing

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"These are officially called substems and sometimes erroneously infixes, even by the USAN Council itself." is an assertion not existing in the source and should be removed. -Mys_721tx (talk) 19:02, 6 December 2020 (UTC)Reply