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. 2001 Oct 15;194(8):1165–1170. doi: 10.1084/jem.194.8.1165

Table 1.

Specificity of HEL48–61 Reactive T Cells

HEL48–61
N59 D59 βD59
Type A CP4.1 ++ ++ ++
CP4.22 +++ +/− ++
3A9 +++
ALV11 ++
Type B ALV48 ++ +++ +
DAV21 ++ +++ +/−
CP3.43 +++ +++ ++
CP3.42 +++ +++ ++
CP3.12 ++ ++ +
B10A8.4 +++ +/− +++
CP1.9 +++ + +
CP1.7 +++ +++ +
CP1.17 +++ +++ ++
CP3.11 +++ ++
CP4.17 ++ + +
MLA11.2 +++ +/−
B61.6 +++
MLC10.22 ++
CP2.11 ++
B10A6.5 +++
Isoaspartyl Iso.187 ++
Iso.210 ++
Iso.198 + ++
Iso.203 +++ + +++
Iso.156 +++ +++

Patterns of reactivities to peptides among type A and B T cells. Type A T cell hybridomas recognize native HEL and HEL48–61 N59 with similar sensitivity, while type B hybridomas are at least 100-fold more sensitive to peptide than to native HEL. Shown here is a list of T cell hybridomas that follow the criteria for A and B T cells. References 3 and 4 have reported on the reactivity of many of these. The “Iso” series of hybridomas were generated by immunization with HEL48–61βD59. All hybridomas were tested against the following synthetic peptides: HEL48–61 N59 (indicated as N59), HEL48–61D59 (D59), or HEL48–61βD59 (βD59). For easier comparison, the sensitivity of the hybridomas to the given peptides are represented as: +++ for 0.1 μM or less, ++ for 1–10 μM, + for greater than 10 μM, +/− for trace response, − for no response at the highest concentration tested.