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Study · Not a test of the peptide alone · 1992

7 results

Combination therapy with thymosin alpha 1 potentiates the anti-tumor activity of interleukin-2 with cyclophosphamide in the treatment of the Lewis lung carcinoma in mice.

Mastino A, Favalli C, Grelli S, Rasi G, Pica F, Goldstein AL, Garaci E

International journal of cancer1 Feb 1992Cited by 38 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study7

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone7

In this study, Thymosin alpha-1 was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Thymosin alpha-1.

  1. 01AnimalNot a test of Thymosin alpha-1 aloneAnimal study (in vivo)Efficacy outcome

    In mice with Lewis lung carcinoma, thymosin alpha‑1 plus IL-2 given after cyclophosphamide induced complete tumor regression in all mice studied.

    In plain wordsIn mice with lung cancer, thymosin alpha‑1 plus IL-2 after chemotherapy cleared the tumour in all mice studied.

    Outcome
    DecreaseComplete tumor regression
    Study

    mousen: not reported in source

    C57Bl/6NCrlBR mice with Lewis lung carcinoma
    Outcome group
    Tumor growth · Cancer

    Source sentences

    Summary
    Combined administration of T alpha 1 plus IL-2, after CY treatment, was much more effective than use of each biological response modifier (BRM) alone, and induced complete tumor regression in all of the mice studied.
    1 context sentence
    Summary · context
    In this study we have investigated the effects of thymosin alpha 1 (T alpha 1) and interleukin-2 (IL-2), singly or in combination with cyclophosphamide (CY), on tumor growth, survival and cytotoxicity in C57Bl/6NCrlBR mice with Lewis lung carcinoma (3LL).

    In this study, Thymosin alpha-1 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin alpha-1.

  2. 02AnimalNot a test of Thymosin alpha-1 aloneAnimal study (in vivo)Efficacy outcome

    In mice with Lewis lung carcinoma, thymosin alpha‑1 plus IL-2 after cyclophosphamide was much more effective than each biological response modifier alone.

    In plain wordsIn mice with lung cancer, thymosin alpha‑1 plus IL-2 after chemotherapy worked much better than either one alone.

    Outcome
    DecreaseTumor response of combination versus each agent alone
    Study

    mousen: not reported in source

    C57Bl/6NCrlBR mice with Lewis lung carcinoma
    Comparator
    Thymosin alpha 1 alone; IL-2 alone
    Outcome group
    Tumor growth · Cancer

    Source sentences

    Summary
    Combined administration of T alpha 1 plus IL-2, after CY treatment, was much more effective than use of each biological response modifier (BRM) alone
    1 context sentence
    Summary · context
    In this study we have investigated the effects of thymosin alpha 1 (T alpha 1) and interleukin-2 (IL-2), singly or in combination with cyclophosphamide (CY), on tumor growth, survival and cytotoxicity in C57Bl/6NCrlBR mice with Lewis lung carcinoma (3LL).

    In this study, Thymosin alpha-1 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin alpha-1.

  3. 03AnimalNot a test of Thymosin alpha-1 aloneAnimal study (in vivo)Efficacy outcome

    In mice with Lewis lung carcinoma, thymosin alpha‑1 plus IL-2 without cyclophosphamide only slightly reduced the rate of tumor growth.

    In plain wordsIn mice with lung cancer, thymosin alpha‑1 plus IL-2 without chemotherapy slowed tumour growth only slightly.

    Outcome
    DecreaseTumor growth rate with combination immunotherapy without cyclophosphamide
    Study

    mousen: not reported in source

    C57Bl/6NCrlBR mice with Lewis lung carcinoma
    Outcome group
    Tumor growth · Cancer

    Source sentences

    Summary
    Combination immunotherapy alone without CY only slightly reduced the rate of tumor growth
    1 context sentence
    Summary · context
    In this study we have investigated the effects of thymosin alpha 1 (T alpha 1) and interleukin-2 (IL-2), singly or in combination with cyclophosphamide (CY), on tumor growth, survival and cytotoxicity in C57Bl/6NCrlBR mice with Lewis lung carcinoma (3LL).

    In this study, Thymosin alpha-1 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin alpha-1.

  4. 04AnimalNot a test of Thymosin alpha-1 aloneAnimal study (in vivo)Mechanism

    In mice with Lewis lung carcinoma, thymosin alpha‑1 plus IL-2 and cyclophosphamide increased the cytotoxicity of spleen cells.

    In plain wordsIn mice with lung cancer, thymosin alpha‑1 plus IL-2 and chemotherapy increased the killing activity of spleen cells.

    Outcome
    IncreaseCytotoxicity of spleen cells
    Study

    mousen: not reported in source

    C57Bl/6NCrlBR mice with Lewis lung carcinoma
    Outcome group
    Immune response · Cancer

    Source sentences

    Summary
    Combined chemo-immunotherapy also increased the cytotoxicity of spleen cells
    1 context sentence
    Summary · context
    In this study we have investigated the effects of thymosin alpha 1 (T alpha 1) and interleukin-2 (IL-2), singly or in combination with cyclophosphamide (CY), on tumor growth, survival and cytotoxicity in C57Bl/6NCrlBR mice with Lewis lung carcinoma (3LL).

    In this study, Thymosin alpha-1 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin alpha-1.

  5. 05AnimalNot a test of Thymosin alpha-1 aloneAnimal study (in vivo)Efficacy outcome

    In mice with Lewis lung carcinoma, thymosin alpha‑1 plus IL-2 and cyclophosphamide markedly enhanced long-term survival in all treated animals.

    In plain wordsIn mice with lung cancer, thymosin alpha‑1 plus IL-2 and chemotherapy greatly improved long-term survival in all treated animals.

    Outcome
    IncreaseLong-term survival
    Study

    mousen: not reported in source

    C57Bl/6NCrlBR mice with Lewis lung carcinoma
    Outcome group
    Mortality · Cancer

    Source sentences

    Summary
    markedly enhanced long-term survival in all treated animals.
    1 context sentence
    Summary · context
    In this study we have investigated the effects of thymosin alpha 1 (T alpha 1) and interleukin-2 (IL-2), singly or in combination with cyclophosphamide (CY), on tumor growth, survival and cytotoxicity in C57Bl/6NCrlBR mice with Lewis lung carcinoma (3LL).

    In this study, Thymosin alpha-1 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin alpha-1.

  6. 06AnimalNot a test of Thymosin alpha-1 aloneAnimal study (in vivo)Mechanism

    In mice with Lewis lung carcinoma, depletion of immune cells by irradiation or antibodies against T cells or NK cells abolished the positive response to the combination therapy.

    In plain wordsIn mice with lung cancer, removing immune cells cancelled the benefit of the combination treatment.

    Outcome
    DecreaseResponse to combination therapy after immune cell depletion
    Study

    mousen: not reported in source

    C57Bl/6NCrlBR mice with Lewis lung carcinoma
    Outcome group
    Immune response · Cancer

    Source sentences

    Summary
    Depletion of immune cells, using either total-body sub-lethal irradiation (400 rads) or antibodies directed against T-cell (anti-CD4 and CD8) or NK-cell (anti-asialo GM1) populations, abolished the positive response to combination therapy.
    1 context sentence
    Summary · context
    In this study we have investigated the effects of thymosin alpha 1 (T alpha 1) and interleukin-2 (IL-2), singly or in combination with cyclophosphamide (CY), on tumor growth, survival and cytotoxicity in C57Bl/6NCrlBR mice with Lewis lung carcinoma (3LL).

    In this study, Thymosin alpha-1 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin alpha-1.

  7. 07AnimalNot a test of Thymosin alpha-1 aloneAnimal study (in vivo)Mechanism

    In mice with Lewis lung carcinoma, tumors from the combination chemo-immunotherapy group showed many infiltrating lymphoid cells around a circumscribed area of necrosis.

    In plain wordsIn mice with lung cancer, tumours treated with the combination contained many immune cells around dead tissue.

    Outcome
    Not applicableTumor histology after combination chemo-immunotherapy
    Study

    mousen: not reported in source

    C57Bl/6NCrlBR mice with Lewis lung carcinoma
    Outcome group
    Immune response · Cancer

    Source sentences

    Summary
    Histological analysis of the tumors obtained from mice treated with combination chemo-immunotherapy revealed a high number of infiltrating lymphoid cells surrounding a well-circumscribed area of necrosis consisting solely of dead cells.
    1 context sentence
    Summary · context
    In this study we have investigated the effects of thymosin alpha 1 (T alpha 1) and interleukin-2 (IL-2), singly or in combination with cyclophosphamide (CY), on tumor growth, survival and cytotoxicity in C57Bl/6NCrlBR mice with Lewis lung carcinoma (3LL).

    In this study, Thymosin alpha-1 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin alpha-1.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 3Current

    10 Oct 2026, 08:55 UTC

    Study results updated

  2. Version 2

    9 Oct 2026, 03:03 UTC

    Study data updated · source update from Europe PMC

  3. Version 1

    9 Oct 2026, 03:02 UTC

    First added · source update from Europe PMC

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