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Antigenic peptides are **short sequences of amino acids derived from larger proteins or antigens that stimulate the adaptive immune response**[1]. These peptides are recognized by T-cell receptors or antibodies, triggering T cells (and sometimes B cells) to expand and mediate immune responses. Antigenic peptides originate from pathogens, tumor cells, or self-proteins (in autoimmunity), and are processed and presented on cell surfaces by major histocompatibility complexes (MHC class I or II)[1][3][5][7][8]. They can be designed synthetically for use in **peptide vaccines**, cancer immunotherapies, and tolerance-inducing therapies for autoimmune diseases[2][4][8][9]. Their specificity and immunogenicity are highly dependent on both their amino acid sequence and the MHC alleles of the host[1][2][3][6][8]. The concept is important in immunology, vaccine design, and disease research, but refers to a class of molecules rather than a unique drug target or receptor. Note: For drug targeting, the relevant molecules are usually the **MHC molecules** (which present antigenic peptides) or the **T-cell receptors** (which recognize them), rather than the peptides themselves[3][6][8].
Immune stimulation via MHC presentation (antigenic peptides are processed by antigen-presenting cells, loaded onto MHC molecules, and stimulate T cells) Induction of antibody response (especially if B-cell epitopes) Immune tolerance induction (for tolerogenic peptides in autoimmune therapy)
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