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. 2019 Mar 22;10:526. doi: 10.3389/fimmu.2019.00526

Table 1A.

Cross-reactivity profile of anti-hTNF-alpha VNAR lead constructs compared to commercially available anti-hTNF-alpha mAbs and a pre-clinical VHH TNF30 domain. (A). Binding (B) and Neutralization (N) data obtained in our laboratory.

Human
(bind/neutralize)
B/N
Dog
(B/N)
Cynomolgus
(B/N)
Rat
(B/N)
Mouse
(B/N)
Rabbit
(B/N)
Pig
(B/N)
Human TNF-β
(B/N)
Lead anti-hTNF-α VNARs (D1 & C4) +++/+++ +++/+++ +++/+++ –/– –/– –/– –/– –/–
TNF30
(VHH)
+++/+++ +++/+++ +++/+++ –/– –/– –/– +/+ ++/–
Adalimumab
(Humira®)
+++/+++ +++/+++ +++/+++ –/– ++/++ –/– –/– –/–

+++ denotes strong binding/neutralization activity, ++ moderate; + very weak activity anddenotes no binding/neutralization activity observed. Binding (B) and Neutralization (N). TNF30 is an anti-TNF-α Nanobody™ previously reported in Beirnaert (31).