Table 1.
Patient | CD40L expression | Age | IgM | IgA | IgG | Mutation | Evidence of mutation being disease causing |
1 | Weak | 11 years | H | H | H | Not done | |
2 | Weak | 11 years | L | L | No sample | ||
3 | Weak | 2 months | N | N | N | Not done | |
4 | Weak | 3 months | N | N | N | Not done | |
5 | Weak | 3 years | N | H | Not done | ||
6 | Weak | 15 years | L | L | None found | ||
7 | Weak | 11 years | L | L | L | None found | |
8 | Weak | 13 years | L | L | L | Not done | |
9 | Weak | 18 years | N | N | N | Not done | |
10 | Weak | 45 years | N | H | R | Not done | |
11 | Weak | 5 months | N | N | M | None found | |
12 | Weak | 1 years | None found | ||||
13 | Weak | 1 years | L | Not done | |||
14 | Weak | 32 years | N | L | H | No sample | |
15 | Weak | 1 month | None found | ||||
16 | Weak | 3 months | None found | ||||
17 | Absent | 9 years | L | L | L | W140G (c.418t→g) Exon 5 | Mutation previously described15 |
AC: 4M0002313 C007014 | Disrupts conserved a.a. in TNF homology domain | ||||||
18 | Absent | 18 years | H | L | L | c.444-448gagca→c Exon 5 | Patient previously described16 |
AC: 4M0003613 C002914 | Disrupts reading frame | ||||||
19 | Absent | 13 years | L | L | R | G38R(c.112g→c) Exon 1 | Patient previously described16 |
AC: 4M00018 & 4M0001913 C002814 | Disrupts transmembrane domain | ||||||
20 | Absent | 3 months | H | H | N | No sample | |
21 | Absent | 1 years | N | L | L | c.302-303insA Exon 3 | Reading frame shift |
22 | Absent | 4 months | H | L | L | IVS3+1g→t | May affect splicing |
23 | Absent | 15 years | N | L | R | IVS3-915a→t | May affect splicing |
24 | Absent | 3 years | L | L | L | c.158-161delTAGA Exon 2 | Mutation previously described14 |
25 | Absent | 20 years | H | L | R | c.158-161 delTAGA Exon 2 | Mutation previously described14 |
26 | Absent | 29 years | c.539delA Exon 5 | Reading frame shift | |||
27 | Absent | 29 years | H | L | L | c.508-516delTATATCTAT Exon 5 | 3 a.a. deletion from TNF homology domain |
28 | Absent | 3 years | N | L | L | None found | |
29 | Absent | 1 years | c.521-522delAA Exon 5 | Reading frame shift | |||
30 | Absent | 2 months | N | L | M | Q174R (c.521a→g) Exon 5 | Relative previously described.16 Arisen de novo |
AC: 4M0002513 C003814* | Great grandmother did not carry the mutation | ||||||
31 | Absent | 11 years | H | L | T254M (c.761c→t) Exon 5 | Mutation previously described16 | |
AC: 4M00021 & 4M0002213 | Not seen in 100 normal chromosomes | ||||||
32 | Absent | 2 months | c.242-243insT Exon 2 | Relative previously described16 | |||
AC: 4M0004713 C000814 | |||||||
33 | Absent | 10 years | H | L | del ex 5 Exon 5 | Mutation previously described16 | |
AC: 4M0003513 | |||||||
34 | Absent | 16 years | L | L | R | G257S (c. 769g→a) Exon 5 | Patient previously described14,16 |
AC: 4M0002013 C003014 | Disrupts conserved a.a. in TNF homology domain | ||||||
35 | Absent | 29 years | T254M (c.761c→t) Exon 5 | Mutation previously described14 | |||
Not found in 100 normal X chromosomes | |||||||
36 | Absent | 4 months | N | L | L | c.511-512delAT Exon 5 | Reading frame shift |
37 | Absent | 13 years | H | L | L155P (c.464t→c) Exon 5 | Mutation previously described14 | |
Not found in 100 normal X chromosomes | |||||||
3 | Present | 4 months | N | N | M | ||
38 | Present | 7 years | L | L | L | ||
39 | Present | 8 years | L | L | N | ||
40 | Present | 6 years | L | L | L | ||
41 | Present | 5 years | L | L | L | ||
42 | Present | 11 years | N | N | N | ||
43 | Present | 49 years | H | N | N | ||
44 | Present | 20 years | L | L | L | ||
45 | Present | 4 years | N | N | N | ||
46 | Present | 4 years | N | N | N | ||
47 | Present | 9 months | N | L | N | ||
48 | Present | 10 years | N | L | L | ||
49 | Present | 4 months | H | H | N | ||
50 | Present | 19 years | N | N | L | ||
51 | Present | 1 years | |||||
52 | Present | 4 years | N | N | N | ||
53 | Present | 23 years | |||||
54 | Present | 14 years | N | L | N | ||
55 | Present | 7 years | |||||
56 | Present | 7 years | N | N | N | ||
57 | Present | 11 months | N | N | L | ||
58 | Present | 23 years | N | N | L | ||
59 | Present | 12 years | L | L | L | ||
60 | Present | 23 years | N | H | L | ||
61 | Present | 45 years | L | L | L | ||
62 | Present | 23 years | N | N | N | ||
63 | Present | 41 years | H | N | N | ||
64 | Present | 2 months | H | N | H | ||
65 | Present | 8 years | N | N | L |
CD40L expression is described as present, absent, or weak. The age listed is the age of the patient when immunostaining was performed. Immunoglobulin concentrations are listed as high (H), normal (N), low/absent (L), maternal (M), or replacement (R) using age appropriate normal ranges. Mutation data are only presented for TNFSF5 gene analysis—the exon/intron in which the mutation resides is given, together with the reference if previously reported, and CD40Lbase accession number (AC). Mutation nomenclature is according to the nomenclature working group.17 *Accession number for a relative. a.a., amino acid.