Vana Spoulou

Dr. Vana Spoulou

National and Kapodistrian University of Athens, Athens, Greece
orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 January 2019 in Vaccines
Verified
Journal Article
Open access
PDF file
TLTheano Lagousi
Theano Lagousi
PBParaskevi Basdeki
Paraskevi Basdeki
JRJohn Routsias
John Routsias
VSVana Spoulou
Vana Spoulou
Non-serotype-specific protein-based pneumococcal vaccines have received extensive research focus due to the limitations of polysaccharide-based vaccines. Pneumococcal proteins (PnPs), universally expressed among serotypes, may induce broader immune responses, stimulating humoral and cellular immunity, while being easier to manufacture and less expensive. Such an approach has raised issues mainly associated with sequence/level of expression variability, chemical instability, as well as possible undesirable reactogenicity and autoimmune properties. A step forward employs the identification of highly-conserved antigenic regions within PnPs with the potential to retain the benefits of protein antigens. Besides, their low-cost and stable construction facilitates the combination of several antigenic regions or peptides that may impair different stages of pneumococcal disease offering even wider serotype coverage and more efficient protection. This review discusses the up-to-date progress on PnPs that are currently under clinical evaluation and the challenges for their licensure. Focus is given on the progress on the identification of antigenic regions/peptides within PnPs and their evaluation as vaccine candidates, accessing their potential to overcome the issues associated with full-length protein antigens. Particular mention is given of the use of newer delivery system technologies including conjugation to Toll-like receptors (TLRs) and reformulation into nanoparticles to enhance the poor immunogenicity of such antigens.

12 April 2004 in Bone Marrow Transplantation
Verified
Journal Article
Closed access
VSVana Spoulou
Vana Spoulou
MGM Giannaki
M Giannaki
MVM Vounatsou
M Vounatsou
CBC Bakoula
C Bakoula
SGS Grafakos
S Grafakos

31 March 2021 in European Journal of Pediatrics
Verified
Journal Article
Closed access
PDF file
VSVana Spoulou
Vana Spoulou
MNMaria Noni
Maria Noni
DKDimitra-Maria Koukou
Dimitra-Maria Koukou
AKAthanasios Kossyvakis
Athanasios Kossyvakis
Athanasios MichosAthanasios Michos
Athanasios Michos

1 November 2005 in Vaccine
Verified
Journal Article
Closed access
VSVana Spoulou
Vana Spoulou
DTDimitris L. Tsoumas
Dimitris L. Tsoumas
VPVana G. Papaevangelou
Vana G. Papaevangelou
GMGlykeria I. Mostrou
Glykeria I. Mostrou
MTMaria C. Theodoridou
Maria C. Theodoridou

1 September 2000 in The Journal of Infectious Diseases
Verified
Journal Article
Open access
PDF file
VSVana Spoulou
Vana Spoulou
PVPanayiotis Victoratos
Panayiotis Victoratos
JIJohn P. A. Ioannidis
John P. A. Ioannidis
SGStelios Grafakos
Stelios Grafakos
The kinetics of the immune response to the 23-valent pneumococcal polysaccharide vaccine (PPV) were studied in 38 children who received bone marrow t

24 November 2023 in Vaccines
Verified
Journal Article
Open access
PDF file
KFKristen Feemster
Kristen Feemster
JWJessica Weaver
Jessica Weaver
UBUlrike K Kirsten Buchwald
Ulrike K Kirsten Buchwald
NBNatalie Banniettis
Natalie Banniettis
KCKara S. Cox
Kara S. Cox
VSVana Spoulou
Vana Spoulou
Globally, Streptococcus pneumoniae is a leading cause of vaccine-preventable morbidity and mortality in infants and children. In recent decades, large-scale pediatric immunization programs have substantially reduced the incidence of invasive pneumococcal disease. Despite this, residual vaccine-type pneumococcal disease remains in the form of vaccine breakthrough and vaccine failure. This targeted literature review aims to discuss aspects of vaccine breakthrough and failure in infants and children, including disease epidemiology, clinical presentation, risk factors, vaccination schedules, vaccine serotypes, correlates of protection, comorbidities, disease surveillance, and potential implications for future vaccine development.