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Science 22 March 1996: Vol. 271. no. 5256, pp. 1728 - 1730 DOI: 10.1126/science.271.5256.1728
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Reports
Induction of TH1 and TH2
Immunity in Neonatal Mice
Thomas Forsthuber,
Hualin C. Yip,
Paul V. Lehmann
*
The neonatal period has been thought of as a window in ontogeny,
during which the developing immune system is particularly susceptible
to tolerization. In the present study, the classic system for induction
of neonatal tolerance to protein antigens was reexamined in mice. The
presumably tolerogenic protocol was found to trigger a vigorous T
helper cell type 2 (TH2) immune response. Thus,
neonatal ``tolerization'' induces immune deviation, not tolerance
in the immunological sense. Neonates are not immune privileged but
generate TH2 or TH1 responses, depending on the
mode of immunization.
Department of Pathology, Biomedical Research Building, Case
Western Reserve University, Cleveland OH, 44106-4943, USA.
*
To whom correspondence should be addressed.
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- Systemic Administration of Agonist Peptide Blocks the Progression of Spontaneous CD8-Mediated Autoimmune Diabetes in Transgenic Mice Without Bystander Damage.
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J. Immunol.
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- CpG Oligonucleotides Are Potent Adjuvants for the Activation of Autoreactive Encephalitogenic T Cells In Vivo.
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- Neonatal Administration of IL-12 Enhances the Protective Efficacy of Antiviral Vaccines.
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164, 3698-3704
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- Direct Visualization of Cytokine-Producing Recall Antigen-Specific CD4 Memory T Cells in Healthy Individuals and HIV Patients.
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- Synthetic oligodeoxynucleotide containing CpG motif induces an anti-polysaccharide type 1-like immune response after immunization of mice with Haemophilus influenzae type b conjugate vaccine.
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- Interleukin 4-Producing Cd4 T Cells Arise from Different Precursors Depending on the Conditions of Antigen Exposure in Vivo.
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- T Cell Receptor Complementarity Determining Region 3 Length Analysis Reveals the Absence of a Characteristic Public T Cell Repertoire in Neonatal Tolerance: The Response in the "Tolerant" Mouse within the Residual Repertoire Is Quantitatively Similar but Qualitatively Different.
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- Age-Associated Rapid and Stat6-Independent IL-4 Production by NK1-CD4+8- Thymus T Lymphocytes.
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- The Stimulation of Low-Affinity, Nontolerized Clones by Heteroclitic Antigen Analogues Causes the Breaking of Tolerance Established to an Immunodominant T Cell Epitope.
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