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Study of the immunogenicity of trastuzumab in lab animals and Egyptian patients under its treatment / (Record no. 84378)

MARC details
000 -LEADER
fixed length control field 04124nam a2200361 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223032925.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220228s2021 ua dhb f m 000 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency EG-GiCUC
Language of cataloging eng
Transcribing agency EG-GiCUC
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title eng
049 ## - LOCAL HOLDINGS (OCLC)
Holding library Deposite
097 ## - Thesis Degree
Thesis Level M.Sc
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Classification number Cai01.08.06.M.Sc.2021.Lo.S.
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Lobna Abdelaziz Mohamed Kilany
245 10 - TITLE STATEMENT
Title Study of the immunogenicity of trastuzumab in lab animals and Egyptian patients under its treatment /
Statement of responsibility, etc. Lobna Abdelaziz Mohamed kilany ; Supervised Hamdallah Hafez Zedan , Mohammad Mabrouk Aboulwafa , Ayman Abdelsameea Gaber
246 15 - VARYING FORM OF TITLE
Title proper/short title دراسة التأثيرالمناعى للتراستوزوماب فى حيوانات التجارب وفى المرضى المصريين المستخدم فى علاجهم
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Lobna Abdelaziz Mohamed kilany ,
Date of publication, distribution, etc. 2021
300 ## - PHYSICAL DESCRIPTION
Extent 101 P. :
Other physical details charts , facsmiles , maps ;
Dimensions 25cm
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Microbiology and Immunology
520 ## - SUMMARY, ETC.
Summary, etc. Immunogenicity is a major challenge in drug development and patient care. Clinicians and regulators are familiar with immunogenicity concerns of therapeutics, growth factors, and enzyme replacements. Unlike small molecule therapeutics, the biological therapeutic agents are likely to trigger undesirable immunogenic responses against themselves upon their administration. This imparts a problem that has to be considered upon judging their risk-benefit ratio.The development of monoclonal antibodies (mAbs) counts as one of the major medical steps forward, opening up endless possibilities for research, diagnosis, and treatment of a wide range of various diseases and disorders. Development of both humanized and fully human mAbs was expected to be non-immunogenic, that allow repeated administration without any anti-drug antibodies (ADA) responses. Unfortunately, these expectations were proven to be unrealistic. They fail to completely eliminate mAb immunogenicity and ADA formation; they have reduced the extreme immunogenicity associated with murine origin mAbs, but still, they have shown to induce antibodies that sometimes have an impact on clinical outcomes. Accurate ADA detection is necessary, to provide sufficient information for patient monitoring and clinical intervention. However, assays of ADAs that are developed against mAbs have more challenges as both the analytes and antigens (mAbs) are antibodies. In this study, we tested the immunogenicity developed in patients sera due to the use of trastuzumab and that developed in laboratory animals injected with this recombinant humanized IgG1 monoclonal antibody(trastuzumab). The trastuzumab immunogenicity was assessed in blood samples using an in vitro approach and in laboratory animalsusingin vivo approach. The in vitro approach depended on both detections of anti-trastuzumab antibody (Ab) levels in patients' serum samples withdrawn at different points during the trastuzumab treatment course; and measurement of neutralizing activity of these ADAs using MTT cytotoxicity assay against MCF-7 cell line. The detection of anti-trastuzumab Abs was carried out using the affinity capture elution (ACE) assay methodin both approaches. In vitro analysis of patients' sera for antibodies developed against trastuzumab revealed that this monoclonal antibody has low immunogenicity. Only 1% of samples showed high levels of anti-trastuzumab antibodies which might affect the treatment course. In vivo immunogenicity testing in mice showed also low immunogenicity of trastuzumab that could support the relevant clinical dataapplied in this study
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Microbiology
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Immunogenicity
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Laboratory animals
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Monoclonal Abs
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Ayman Abdel Sameea Gaber ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Hamdallah Hafez Zedan ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Mohammad Mabrouk Aboulwafa ,
Relator term
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://172.23.153.220/th.pdf">http://172.23.153.220/th.pdf</a>
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Enas
Reviser Revisor
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Norhan
Reviser Cataloger
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Thesis
Holdings
Source of classification or shelving scheme Not for loan Home library Current library Date acquired Full call number Barcode Date last seen Koha item type Copy number
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 11.02.2024 Cai01.08.06.M.Sc.2021.Lo.S. 01010110085488000 22.09.2023 Thesis  
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.08.06.M.Sc.2021.Lo.S. 01020110085488000 22.09.2023 CD - Rom 85488.CD