# Peptide Vaccine: Progress and Challenges

**Authors:** Weidang Li, Medha D. Joshi, Smita Singhania, Kyle H. Ramsey, Ashlesh K. Murthy

PMC · DOI: 10.3390/vaccines2030515 · Vaccines · 2014-07-02

## TL;DR

Peptide vaccines offer a targeted immune response with fewer side effects but require special delivery methods to be effective.

## Contribution

The paper reviews progress in peptide vaccine development and highlights challenges in delivery and safety.

## Key findings

- Peptide vaccines can induce targeted immune responses without unnecessary antigenic load.
- Particulate carriers are needed to enhance the immunogenicity of peptide vaccines.
- Safety concerns arise when combining particulate carriers with peptide vaccines.

## Abstract

Conventional vaccine strategies have been highly efficacious for several decades in reducing mortality and morbidity due to infectious diseases. The bane of conventional vaccines, such as those that include whole organisms or large proteins, appear to be the inclusion of unnecessary antigenic load that, not only contributes little to the protective immune response, but complicates the situation by inducing allergenic and/or reactogenic responses. Peptide vaccines are an attractive alternative strategy that relies on usage of short peptide fragments to engineer the induction of highly targeted immune responses, consequently avoiding allergenic and/or reactogenic sequences. Conversely, peptide vaccines used in isolation are often weakly immunogenic and require particulate carriers for delivery and adjuvanting. In this article, we discuss the specific advantages and considerations in targeted induction of immune responses by peptide vaccines and progresses in the development of such vaccines against various diseases. Additionally, we also discuss the development of particulate carrier strategies and the inherent challenges with regard to safety when combining such technologies with peptide vaccines.

## Full-text entities

- **Genes:** NEU1 (neuraminidase 1) [NCBI Gene 4758] {aka NANH, NEU, SIAL1}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, MUC1 (mucin 1, cell surface associated) [NCBI Gene 4582] {aka ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3}, HLA-S (major histocompatibility complex, class I, S (pseudogene)) [NCBI Gene 267015] {aka HLA-17}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, Igha (immunoglobulin heavy constant alpha) [NCBI Gene 238447] {aka IgA, Igh-2}, Gnrh1 (gonadotropin releasing hormone 1) [NCBI Gene 14714] {aka Gnrh, Gnrh2, LHRH, Lhrh1, Lnrh, hpg}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Nelfcd (negative elongation factor complex member C/D, Th1l) [NCBI Gene 57314] {aka 2410003I03Rik, NELF-D, Th1, Th1l}, Igh-V7183 (immunoglobulin heavy chain (V7183 family)) [NCBI Gene 16059] {aka B9-scFv, IgG, IgH, IgVH1(VSG), VH7183, VI24H}, Nil (neonatal intestinal lipidosis) [NCBI Gene 110093] {aka Ml}, CS (citrate synthase) [NCBI Gene 1431], CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, Muc1 (mucin 1, transmembrane) [NCBI Gene 17829] {aka CD227, EMA, Muc-1}, Alb (albumin) [NCBI Gene 11657] {aka Alb-1, Alb1, BCL001, BCL002, BPL001}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PMEL (premelanosome protein) [NCBI Gene 6490] {aka D12S53E, HMB-45, HMB45, ME20, ME20-M, ME20M}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** infectious diseases (MESH:D003141), pancreatic cancer (MESH:D010190), Influenza (MESH:D007251), inflammatory (MESH:D007249), Diabetes (MESH:D003920), Hand Foot and Mouth disease (MESH:D006232), Anti-cancer (MESH:D009369), non-small cell lung cancer (MESH:D002289), EAE (MESH:D004679), Asthma (MESH:D001249), autoimmune encephalomyelitis (MESH:D004681), HSV-1 infection (MESH:D006561), Cat allergy (MESH:D002371), severe acute respiratory syndrome (SARS)-associated coronavirus (MESH:D000086382), Pneumonia (MESH:D011014), Insulin dependent diabetes mellitus (MESH:D003922), swine fever (MESH:D006691), necrotic ulcers (MESH:D014456), infections (MESH:D007239), Tuberculosis (MESH:D014376), Pneumococcal (MESH:D011008), cutaneous T-cell lymphoma (MESH:D016410), Melanoma (MESH:D008545), foot and mouth disease (MESH:D005536), hepatocellular carcinoma (MESH:D006528), adverse drug reactions (MESH:D064420), events (MESH:D002318), Alzheimer's disease (MESH:D000544), One (MESH:D009140), Allergy (MESH:D004342), Malaria (MESH:D008288), B-Cell chronic lymphocytic leukemia (MESH:D015451), CMV (MESH:D003586)
- **Species:** LCMV [taxon 11623], Pyroglyphidae (house-dust mites, family) [taxon 6952], Human papillomavirus (species) [taxon 10566], Sendai virus [taxon 11191], Plasmodium vivax (malaria parasite P. vivax, species) [taxon 5855], Human immunodeficiency virus (species) [taxon 12721], HCV [taxon 11103], Cytomegalovirus (genus) [taxon 10358], Homo sapiens (human, species) [taxon 9606], Hepatitis B virus (no rank) [taxon 10407], Canis lupus familiaris (dog, subspecies) [taxon 9615], Human papillomavirus 16 (serotype) [taxon 333760], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Mus musculus (house mouse, species) [taxon 10090], Bacillus anthracis (anthrax bacterium, species) [taxon 1392], Canine parvovirus (no rank) [taxon 10788], Brachyspira hyodysenteriae (species) [taxon 159]

## Full text

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## Figures

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## References

117 references — full list in the complete paper: https://tomesphere.com/paper/PMC4494216/full.md

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Source: https://tomesphere.com/paper/PMC4494216