Evaluate a New Shigella Sonnei Vaccine Administered Either by Intradermal, Intranasal or Intramuscular Route in Healthy Adults

Inclusion Criteria: 1. Males and females of age ≥18 years to ≤45 years. 2. Individuals who, after the nature of the study have been explained to them, have given written consent according to local regulatory requirements. 3. Individuals in good health as determined by the outcome of medical history, physical examination, hematology, renal, bone and liver panels (including negative for agglutination testing of S. sonnei), urinalysis and clinical judgment of the investigator. 4. If women of childbearing potential, have a negative pregnancy test prior to study vaccination and willingness to use acceptable contraceptive measures for the entire study duration. 5. Individuals available for follow-up for the duration of the study. 6. Individuals registered with a general practitioner. Exclusion Criteria: 1. Individuals with a history of recurrent wheezing, asthma, respiratory allergies, allergic rhinitis, nasal surgery or significant nasal abnormalities (e.g. polyps), and Bell's palsy. Presence of nasal piercings. Symptoms of upper respiratory tract infection within 3 days of intended study vaccination is a temporary exclusion criterion. 2. Individuals unwilling to abstain from medications or other agents that are applied via the nasal route from 24 hours prior to each nasal dosing through to the safety assessment 1 week later. 3. Individuals with behavioral or cognitive impairment or psychiatric disease that, in the opinion of the investigator, may interfere with the subject's ability to participate in the study. 4. Individuals with any progressive or severe neurological disorder, seizure disorder or Guillain-Barré syndrome. 5. Individuals who are not able to understand and to follow all required study procedures for the whole period of the study. 6. Individuals with history of any illness that, in the opinion of the investigator, might interfere with the results of the study or pose additional risk to the subjects due to participation in the study. 7. Individuals with human leukocyte antigen (HLA) -B27 positive and/or with history of reactive arthritis 8. Individuals with known HIV, HBV and HCV infection or HIV related disease, with history of an autoimmune disorder or any other known or suspected impairment /alteration of the immune system, or under immunosuppressive therapy including use of systemic corticosteroids or chronic use of inhaled high-potency corticosteroids within the previous 30 days, or were in chemotherapy treatment within the past 6 months. 9. Individuals with a known bleeding diathesis, or any condition that may be associated with a prolonged bleeding time. 10. Individuals with any serious chronic or progressive disease according to judgment of the investigator (e.g., neoplasm, insulin dependent diabetes, cardiac, renal or hepatic disease). 11. Individuals who have any malignancy or lymphoproliferative disorder. 12. Individuals with history of allergy to vaccine components. 13. Individuals participating in any clinical trial with another investigational product 90 days prior to first study visit or intent to participate in another clinical study at any time during the conduct of this study. 14. Individuals who received any other vaccines within 4 weeks prior to enrollment in this study or who are planning to receive any vaccine within the entire study duration except influenza vaccination, which is not allowed within the period included between 4 weeks before 1st vaccination and 4 weeks after 3rd vaccination 15. Individuals who have received blood, blood products and/or plasma derivatives including parenteral immunoglobulin preparations in the past 12 weeks. 16. Individuals who are part of study personnel or close family members to the personnel conducting this study or employees of the clinical trial site institution. 17. Individuals with body temperature \> 38.0 degrees Celsius within 3 days of intended study vaccination. 18. BMI \> 30 kg/m2. 19. Individuals with history of substance or alcohol abuse within the past 2 years. 20. Women who are pregnant or breast-feeding or of childbearing age who have not used or do not plan to use acceptable birth control measures, for the duration of the study. 21. Females with history of stillbirth, neonatal loss, or previous infant with anomaly. 22. Individuals who have a previously ascertained or suspected disease caused by S. sonnei or positive S. sonnei serology at screening 23. Individuals who have had household contact with/and or intimate exposure to an individual with laboratory confirmed S. sonnei 24. Any condition, which, in the opinion of the investigator may pose an increased and unreasonable safety risk to the subject if participating to the present study