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Poorten, Thomas (author)
Raymond E. Kuhn (committeeChair)
Miles Silman (committeeMember)
James F. Curran (committeeMember)
Poorten, Thomas
2008-09-28T10:50:41Z (accessioned)
2010-06-18T18:56:49Z (accessioned)
2009-06-13 (available)
2008-09-28T10:50:41Z (available)
2010-06-18T18:56:49Z (available)
2008 (issued)
null (defenseDate)
Biology (discipline)
Wake Forest University (grantor)
MS (level)
The immune system of the African clawed frog, Xenopus laevis, includes nearly the full repertoire of lymphoid organs and immune cell types found in mammals. In contrast to the mammalian immune system, the development of the amphibian immune system occurs in the open environment. Oviparity necessitates a rapid ontogeny of the immune system. X. laevis larvae become immunocompetent about two weeks after fertilization of the egg. During this two-week window, developing larvae cannot mount an immune response to potential pathogens. In the present study, the possibility of maternal transfer of antibodies to eggs was examined. Adult female X. laevis were injected three times at weekly intervals with the hapten-carrier complex, trinitrophenylated bovine serum albumin (TNP-BSA). The sera of immunized frogs demonstrated antibody activity to BSA, TNP-BSA, and, importantly, trinitrophenylated ovalbumin (TNP-OVA) when examined by enzyme-linked immunosorbent assay (ELISA). Reactivity to TNP-OVA confirmed that antibodies were produced against TNP. The adult female frogs were induced to lay eggs by injection of human chorionic gonadotropin. Next, membrane-free extracts of the eggs were treated with protease inhibitors in order to prevent proteolysis of proteins found in the eggs. On analysis by ELISA, it was found that TNP-specific antibodies were present in the egg extracts. This demonstrated the transfer of antigen-specific antibodies from adult females to eggs in X. laevis. Since maternal transfer of antibodies to offspring has been demonstrated in several other vertebrate species, this study provides evidence that this process has been conserved in the gnathostome lineage. (abstract)
http://hdl.handle.net/10339/14651 (uri)
etd-05242008-165611 (oldETDId)
Release the entire work for access only to the Wake Forest University system for one year from the date of approval. After one year, release the entire work for access worldwide, unless I send notification to delay release. (accessRights)
I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to Wake Forest University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. (license)
antibody response
passive immunity
Xenopus laevis
Maternal transfer of antibodies in Xenopus laevis

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