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Protective Epitope Discovery and the Design of MUC1 Based Vaccine for Effective Tumor Protections in Immunotolerant Mice

Wu, Xuanjun (författare)
Yin, Zhaojun (författare)
McKay, Craig (författare)
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Pett, Christian (författare)
Umeå universitet,Kemiska institutionen,Leibniz-Institut für Analytische Wissenschaften−ISAS, Dortmund, Germany
Yu, Jin (författare)
Schorlemer, Manuel (författare)
Leibniz-Institut für Analytische Wissenschaften−ISAS, Dortmund, Germany
Gohl, Trevor (författare)
Sungsuwan, Suttipun (författare)
Ramadan, Sherif (författare)
Baniel, Claire (författare)
Allmon, Anthony (författare)
Das, Rupali (författare)
Westerlind, Ulrika (författare)
Umeå universitet,Kemiska institutionen
Finn, M. G. (författare)
Huang, Xuefei (författare)
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 (creator_code:org_t)
2018-11-06
2018
Engelska.
Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 140:48, s. 16596-16609
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Human mucin-1 (MUC1) is a highly attractive antigen for the development of anticancer vaccines. However, in human clinical trials of multiple MUC1 based vaccines, despite the generation of anti-MUC1 antibodies, the antibodies often failed to exhibit much binding to tumor presumably due to the challenges in inducing protective immune responses in the immunotolerant environment. To design effective MUC1 based vaccines functioning in immunotolerant hosts, vaccine constructs were first synthesized by covalently linking the powerful bacteriophage Qβ carrier with MUC1 glycopeptides containing 20-22 amino acid residues covering one full length of the tandem repeat region of MUC1. However, IgG antibodies elicited by these first generation constructs in tolerant human MUC1 transgenic (Tg) mice did not bind tumor cells strongly. To overcome this, a peptide array has been synthesized. By profiling binding selectivities of antibodies, the long MUC1 glycopeptide was found to contain immunodominant but nonprotective epitopes. Critical insights were obtained into the identity of the key protective epitope. Redesign of the vaccine focusing on the protective epitope led to a new Qβ-MUC1 construct, which was capable of inducing higher levels of anti-MUC1 IgG antibodies in MUC1.Tg mice to react strongly with and kill a wide range of tumor cells compared to the construct containing the gold standard protein carrier, i.e., keyhole limpet hemocyanin. Vaccination with this new Qβ-MUC1 conjugate led to significant protection of MUC1.Tg mice in both metastatic and solid tumor models. The antibodies exhibited remarkable selectivities toward human breast cancer tissues, suggesting its high translational potential.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

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