Inclusion Criteria:

          -  Histologically or cytologically confirmed metastatic or recurrent unresectable solid
             tumor.

          -  HLA-A*02:01 or HLA-A*02:06 positive.

          -  Tumor NY-ESO-1 expression by immunohistochemistry.

          -  No anti-cancer chemotherapy, radiation therapy or immunotherapy within 2 weeks or 5
             half-lives of PBMC harvest.

          -  The treating investigator should consider the patient to have disease that is
             incurable and that the patient would be a reasonable candidate for future treatment
             with TBI-1301.

          -  Patients must have measurable disease, defined as at least one lesion that can be
             accurately measured in at least one dimension (longest diameter to be recorded for
             non-nodal lesions and short axis for nodal lesions) as >10 mm with CT scan, MRI, or
             calipers by clinical exam. Patients must have radiographic evidence of disease
             progression following the most recent line of treatment. Areas of previous radiation
             may not serve as measurable disease unless there is evidence of progression post
             radiation.

          -  ECOG Performance Status 0 or 1.

          -  Age ≥16 years on consent.

          -  Life expectancy greater than 4 months.

          -  The following laboratory requirements must be met (within 14 days prior to phlebotomy
             for generation of TBI-1301):

          -  Absolute neutrophil count (ANC) ≥1.5 x10^9/L (1500/μL) without G-CSF support

          -  WBC ≥ 2.5x10^9/L (2,500/μl)

          -  Lymphocytes ≥ 0.5x10^9/L (500/μl)

          -  Hemoglobin ≥ 80 g/L

          -  Platelets ≥ 75x10^9/L (75,000/μl)

          -  Total bilirubin ≤ 1.5 x upper limit of normal (ULN) (≤2.5X if Gilbert's disease)

          -  AST(SGOT), ALT(SGPT) < 3.0 x ULN (< 5 x ULN with known liver metastases)

          -  Creatinine ≥ 60 ml/min (calculated by Cockcroft and Gault)

          -  Adequate renal function

          -  Consent must be appropriately obtained in accordance with applicable local and
             regulatory requirements.

        Exclusion Criteria:

          -  Uncontrolled intercurrent illnesses or medical conditions that may interfere with
             trial participation such as ongoing or active infection, symptomatic congestive heart
             failure, uncontrolled hypertension, unstable angina pectoris, cardiac arrhythmia,
             severe active peptic ulcer disease or gastritis, or psychiatric illness/social
             situations that would limit compliance with study requirement or compromise the
             ability of the subject to give written informed consent.

          -  Patients who are receiving any other investigational agents.

          -  Active or prior documented autoimmune disease within the past 2 years. NOTE: Subjects
             with vitiligo, Grave's disease, Hashimoto's disease, or psoriasis not requiring
             systemic treatment (within the past 2 years) are not excluded.

          -  Active or prior documented inflammatory bowel disease (eg, Crohn's disease, ulcerative
             colitis).

          -  No evidence of active uncontrolled infection (patients on antibiotics are eligible).

          -  History of primary immunodeficiency.

          -  History of organ transplant that requires use of immunosuppressives.

          -  Known allergy or reaction to a known component of TBI-1301.

          -  Untreated central nervous system metastases requiring concurrent treatment, inclusive
             of but not limited to surgery, radiation, and/or corticosteroids. If treated lesions
             are shown to be stable for 1 month the subject may be eligible.

          -  Other invasive malignancy within 2 years except for noninvasive malignancies such as
             cervical carcinoma in situ, non-melanomatous carcinoma of the skin or ductal carcinoma
             in situ of the breast that has/have been surgically cured.

          -  Current or prior use of immunosuppressive medication within 14 days before phlebotomy,
             with the exceptions of intranasal, topical, and inhaled corticosteroids or systemic
             corticosteroids at physiologic doses not to exceed 10 mg/day of prednisone or
             equivalent. Oral steroid use as premedication to prevent allergic reactions to
             radiologic contrast is allowed.

          -  Any condition that, in the opinion of the investigator, would interfere with the
             evaluation of TBI-1301 or interpretation of subject safety or study results.

          -  Known history of tuberculosis.

          -  HIV positive.

          -  Active HTLV or syphilis infection.

          -  Active hepatitis B infection (hepatitis B surface antigen or HBV DNA positive).

          -  Active hepatitis C infection (if hepatitis C antibody positive, HCV RNA positive).

          -  Has no known active central nervous system metastases and/or carcinomatous meningitis.

          -  Ongoing prior toxicities related to previous anti-cancer treatments (surgery,
             radiotherapy or adjuvant chemo-radiation) must be recovered to < grade 1 or baseline

          -  Pregnant women are excluded.