Skip to main content
Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 2002 Dec;130(3):557–558. doi: 10.1046/j.1365-2249.2002.02040.x

ERRATUM

PMCID: PMC1906539

Chapkin R.S., Arrington J.L., Apanasovich T.V., Carroll, R.J. & McMurray, D.N. Dietary n-3 PUFA affect TcR-mediated activation of purified murine T cells and accessory cell function in co-cultures. Clin Exp Immunol 2002; 130:12–18.

In Fig 1 and Fig 4, the diagonal hatching in the columns was erroneously omitted during printing and these appeared as open columns. The corrected figures are shown below.

Fig. 1.

Fig. 1

The in vitro proliferative response to αCD3/αCD28 of co-cultures of purified T lymphocytes (L) and purified accessory cells (M) isolated from mice fed diets containing different levels of n-3 PUFA for two weeks; lymphocytes from each diet source (LS, LD, LF2, LF4) were co-cultured with accessory cells from each diet source (▪ (M)S, Inline graphic(M)D, Inline graphic(M)F2, □ (M)F4) in a 4 × 4 factorial design; S, Safflower oil diet; F2, 2% Fish oil diet; F4, 4% Fish oil diet; D, DHA-enriched diet; Mean ± SEM (n = 3–5 mice).

Fig. 4.

Fig. 4

The in vitro proliferative response to ConA of co-cultures of purified T lymphocytes (L) and purified accessory cells (M) isolated from mice fed diets containing different levels of n-3 PUFA for two weeks; lymphocytes from each diet source (LS, LD, LF2, LF4) were co-cultured with accessory cells from each diet source (▪ (M)S, Inline graphic(M)D, Inline graphic(M)F2, □ (M)F4) in a 4 × 4 factorial design; S, Safflower oil diet; F2, 2% Fish oil diet; F4, 4% Fish oil diet; D, DHA-enriched diet; Mean ± SEM (n = 3–5 mice); no statistically significant dietary effects were detected.


Articles from Clinical and Experimental Immunology are provided here courtesy of British Society for Immunology

RESOURCES