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Remark 1 From Corollary 1 and by considering Theorem 1, we can easily deduce that the set of generating functions for an efficient presentation can be presented as a single element.
Active anti-cancer immune responses depend on efficient presentation of tumor antigens and co-stimulatory signals by antigen-presenting cells (APCs).
Particles attract antigen presenting cells to the administration site, thereby guaranteeing the efficient presentation of the antigen to the immune system.
However, since P E is given as an efficient presentation, we also need to add a function related to its efficiency.
Efficient presentation of growth factors is one of the great challenges in tissue engineering.
Dendrimer biocompatibility has been evaluated in vitro and in vivo for efficient presentation of biological performance.
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Hence we get the following version of Theorem 2 which deals with efficient presentations.
By Remark 1, it is always true that efficient presentations (even for groups or monoids) are minimal.
Similarly, for any prime p, by choosing either α 11 = p t + 1 ( t ∈ Z + ), α 12 = 0, α 21 = 0 and α 22 = 1 or α 11 = 1, α 21 = 0, α 12 = 0 and α 22 = p t + 1 ( t ∈ Z + ), we can still obtain efficient presentations with the equivalence M 2 p + 1 ≡ M 1 mod p. Further, the representative characteristic polynomial for the related presentation is of the form ν 2 − ( p t + 2 ) ν + p t + 1.
LeY-modified liposomes, with an approximate diameter of 200 nm, were significantly endocytosed by DC-SIGN+ DCs and mediated efficient antigen presentation to CD4+ and CD8+ T cells.
Endocytosis of antigen is not necessarily sufficient to ensure efficient antigen presentation [52].
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