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Study · In vitro (cells) · 1995

11 results

Induction of IgA1 and IgA2 production in immature human fetal B cells and pre-B cells by vasoactive intestinal peptide.

Kimata H, Fujimoto M

Blood1 Apr 1995Cited by 27 (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 study11

9 results from studies that gave the peptide. No result from this study comes from people.

  1. 01LabIn vitro (cells)Efficacy outcome

    In human fetal B cells stimulated with anti-CD40 antibody, VIP induced IgA1 production.

    In plain wordsIn lab tests on human fetal immune cells, VIP caused the cells to make IgA1 antibodies.

    Outcome
    IncreaseIgA1 production, fetal B cells
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    VIP induced IgA1, IgA2, and IgM production in sIgM+, CD19+ fetal B cells stimulated with anti-CD40 monoclonal antibody (MoAb)
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.
  2. 02LabIn vitro (cells)Efficacy outcome

    In human fetal B cells stimulated with anti-CD40 antibody, VIP induced IgA2 production.

    In plain wordsIn lab tests on human fetal immune cells, VIP caused the cells to make IgA2 antibodies.

    Outcome
    IncreaseIgA2 production, fetal B cells
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    VIP induced IgA1, IgA2, and IgM production in sIgM+, CD19+ fetal B cells stimulated with anti-CD40 monoclonal antibody (MoAb)
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.
  3. 03LabIn vitro (cells)Efficacy outcome

    In human fetal B cells stimulated with anti-CD40 antibody, VIP induced IgM production.

    In plain wordsIn lab tests on human fetal immune cells, VIP caused the cells to make IgM antibodies.

    Outcome
    IncreaseIgM production, fetal B cells
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    VIP induced IgA1, IgA2, and IgM production in sIgM+, CD19+ fetal B cells stimulated with anti-CD40 monoclonal antibody (MoAb)
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.
  4. 04LabIn vitro (cells)Efficacy outcome

    In human fetal B cells stimulated with anti-CD40 antibody, VIP did not induce production of IgG1, IgG2, IgG3 or IgG4.

    In plain wordsIn lab tests on human fetal immune cells, VIP did not cause the cells to make IgG antibodies.

    Outcome
    No significant changeIgG1-IgG4 production, fetal B cells
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    without inducing the production of IgG1, IgG2, IgG3, IgG4, or IgE.
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.
  5. 05LabIn vitro (cells)Efficacy outcome

    In human fetal B cells stimulated with anti-CD40 antibody, VIP did not induce IgE production.

    In plain wordsIn lab tests on human fetal immune cells, VIP did not cause the cells to make IgE antibodies.

    Outcome
    No significant changeIgE production, fetal B cells
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    without inducing the production of IgG1, IgG2, IgG3, IgG4, or IgE.
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.
  6. 06LabIn vitro (cells)Efficacy outcome

    In human pre-B cells treated with anti-CD40 antibody, VIP also induced IgA1 production.

    In plain wordsIn lab tests on human immature immune cells, VIP caused the cells to make IgA1 antibodies.

    Outcome
    IncreaseIgA1 production, pre-B cells
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The anti-CD40 MoAb plus VIP also induced IgA1, IgA2, and IgM production in sIgM-, CD19+ pre-B cells
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.
  7. 07LabIn vitro (cells)Efficacy outcome

    In human pre-B cells treated with anti-CD40 antibody, VIP also induced IgA2 production.

    In plain wordsIn lab tests on human immature immune cells, VIP caused the cells to make IgA2 antibodies.

    Outcome
    IncreaseIgA2 production, pre-B cells
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The anti-CD40 MoAb plus VIP also induced IgA1, IgA2, and IgM production in sIgM-, CD19+ pre-B cells
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.
  8. 08LabIn vitro (cells)Efficacy outcome

    In human pre-B cells treated with anti-CD40 antibody, VIP also induced IgM production.

    In plain wordsIn lab tests on human immature immune cells, VIP caused the cells to make IgM antibodies.

    Outcome
    IncreaseIgM production, pre-B cells
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The anti-CD40 MoAb plus VIP also induced IgA1, IgA2, and IgM production in sIgM-, CD19+ pre-B cells
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.
  9. 09LabIn vitro (cells)Efficacy outcome

    In human fetal B cells and pre-B cells, VIP induction of IgA was specific, because somatostatin or substance P with anti-CD40 antibody had no effect.

    In plain wordsIn lab tests on human immune cells, VIP caused antibody production, but somatostatin and substance P did not.

    Outcome
    IncreaseSpecificity of VIP-induced IgA compared with other neuropeptides
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Comparator
    Somatostatin or substance P
    Outcome group
    Immune response · Immune and inflammation
    Studied dose
    Dose not stated

    Source sentences

    Summary
    This induction by VIP was specific, as the anti-CD40 MoAb plus other neuropeptides [ie, somatostatin (SOM) or substance P (SP)] had no effect
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.

Studies that did not test the peptide alone2

In this study, Vasoactive intestinal peptide (VIP, aviptadil) 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 Vasoactive intestinal peptide (VIP, aviptadil).

  1. 10LabNot a test of Vasoactive intestinal peptide (VIP, aviptadil) aloneIn vitro (cells)Efficacy outcome

    In human pre-B cells, immunoglobulin production induced by anti-CD40 antibody plus VIP was enhanced by the addition of interleukin-7.

    In plain wordsIn lab tests on human immature immune cells, adding interleukin-7 to anti-CD40 and VIP increased antibody production further.

    Outcome
    IncreaseEnhancement of pre-B cell Ig production by IL-7
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Outcome group
    Immune response · Immune and inflammation

    Source sentences

    Summary
    which was enhanced by the addition of interleukin-7 (IL-7).
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.

    In this study, Vasoactive intestinal peptide (VIP, aviptadil) 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 Vasoactive intestinal peptide (VIP, aviptadil).

  2. 11LabNot a test of Vasoactive intestinal peptide (VIP, aviptadil) aloneIn vitro (cells)Efficacy outcome

    In human fetal B cells and pre-B cells, a VIP antagonist specifically blocked the induction of IgA by VIP.

    In plain wordsIn lab tests on human immune cells, a VIP blocker stopped the antibody production that VIP caused.

    Outcome
    Not applicableBlock of VIP-induced IgA production by a VIP antagonist
    Study

    humann: not reported in source

    Human fetal B cells and bone marrow-derived pre-B cells stimulated with anti-CD40
    Comparator
    VIP antagonist
    Outcome group
    Immune response · Immune and inflammation

    Source sentences

    Summary
    and moreover, the induction was specifically blocked by a VIP antagonist.
    1 context sentence
    Summary · context
    We studied the effects of vasoactive intestinal peptide (VIP) on IgA1 and IgA2 production in human fetal B cells and pre-B cells derived from bone marrow.

    In this study, Vasoactive intestinal peptide (VIP, aviptadil) 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 Vasoactive intestinal peptide (VIP, aviptadil).

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 2Current

    12 Oct 2026, 12:58 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 12:41 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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